Faster access than browser!
89 relations: Active laser medium, Alpha-Phenylcinnamic acid, Aniline, Aromatic sulfonation, Arthur George Green, Atomic orbital, Auguste Laurent, Azo dye, Benzaldehyde, Benzoic acid, Benzoin, Bulletin of the Chemical Society of Japan, Carbon tetrachloride, Cengage, Chemical equilibrium, Chemical Reviews, Chemische Berichte, Chirality, Cis–trans isomerism, Conjugated system, David Van Nostrand, Derivative (chemistry), Diarylethene, Dienestrol, Diethylstilbestrol, Diol, Disodium 4,4'-dinitrostilbene-2,2'-disulfonate, Double bond, Dye, Dye laser, E-Z notation, Elsevier, Enantiomer, Enantiomeric excess, Epoxide, Estrogen, Ethylene, Ethylene oxide, Fosfestrol, Greek language, Halogen addition reaction, Halonium ion, Heck reaction, Inorganic Chemistry (journal), Iodobenzene, Journal of Chemical Physics, Journal of Organic Chemistry, Journal of the American Chemical Society, Karl Barry Sharpless, Lemieux–Johnson oxidation, ..., Mechanistic organic photochemistry, Meso compound, Moiety (chemistry), Nitromethane, Novartis, Optical brightener, Organic compound, Organic Reactions, Ozonolysis, Phenanthrene, Phenyl group, Phosphor, Photochemistry, Potassium permanganate, Pterostilbene, Racemic mixture, Relative permittivity, Resveratrol, Richard F. Heck, Scintillator, Sharpless asymmetric dihydroxylation, Sodium hypochlorite, Springer Science+Business Media, Stereoisomerism, Steric effects, Stilbenoid, Stilbestrol, Structural formula, Styrene, Substituent, Tert-Butyl hydroperoxide, Tetrahedron Letters, Ullmann's Encyclopedia of Industrial Chemistry, Upjohn dihydroxylation, Vicinal (chemistry), Wiley-VCH, (Z)-Stilbene, 1,4-Dioxane, 4-Nitrotoluene. Expand index (39 more) »
Active laser medium
The active laser medium (also called gain medium or lasing medium) is the source of optical gain within a laser.
New!!: (E)-Stilbene and Active laser medium · See more »
Alpha-Phenylcinnamic acid
α-Phenylcinnamic acid is a phenylpropanoid, or, more specifically, a derivative of cinnamic acid.
New!!: (E)-Stilbene and Alpha-Phenylcinnamic acid · See more »
Aniline
Aniline is an organic compound with the formula C6H5NH2.
New!!: (E)-Stilbene and Aniline · See more »
Aromatic sulfonation
Aromatic sulfonation is an organic reaction in which a hydrogen atom on an arene is replaced by a sulfonic acid functional group in an electrophilic aromatic substitution.
New!!: (E)-Stilbene and Aromatic sulfonation · See more »
Arthur George Green
Arthur George Green FRS (1864 – 12 September 1941) was a British organic chemist.
New!!: (E)-Stilbene and Arthur George Green · See more »
Atomic orbital
In quantum mechanics, an atomic orbital is a mathematical function that describes the wave-like behavior of either one electron or a pair of electrons in an atom.
New!!: (E)-Stilbene and Atomic orbital · See more »
Auguste Laurent
Auguste Laurent (14 November 1807 – 15 April 1853) was a French chemist who helped in the founding of organic chemistry with his discoveries of anthracene, phthalic acid, and carbolic acid.
New!!: (E)-Stilbene and Auguste Laurent · See more »
Azo dye
Azo dyes are organic compounds bearing the functional group R−N.
New!!: (E)-Stilbene and Azo dye · See more »
Benzaldehyde
Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent.
New!!: (E)-Stilbene and Benzaldehyde · See more »
Benzoic acid
Benzoic acid, C7H6O2 (or C6H5COOH), is a colorless crystalline solid and a simple aromatic carboxylic acid.
New!!: (E)-Stilbene and Benzoic acid · See more »
Benzoin
Benzoin is an organic compound with the formula PhCH(OH)C(O)Ph.
New!!: (E)-Stilbene and Benzoin · See more »
Bulletin of the Chemical Society of Japan
Founded in 1926, the Bulletin of the Chemical Society of Japan is a scientific journal published by the Chemical Society of Japan.
New!!: (E)-Stilbene and Bulletin of the Chemical Society of Japan · See more »
Carbon tetrachloride
Carbon tetrachloride, also known by many other names (the most notable being tetrachloromethane, also recognized by the IUPAC, carbon tet in the cleaning industry, Halon-104 in firefighting, and Refrigerant-10 in HVACR) is an organic compound with the chemical formula CCl4.
New!!: (E)-Stilbene and Carbon tetrachloride · See more »
Cengage
Cengage is an educational content, technology, and services company for the higher education, K-12, professional, and library markets worldwide.
New!!: (E)-Stilbene and Cengage · See more »
Chemical equilibrium
In a chemical reaction, chemical equilibrium is the state in which both reactants and products are present in concentrations which have no further tendency to change with time, so that there is no observable change in the properties of the system.
New!!: (E)-Stilbene and Chemical equilibrium · See more »
Chemical Reviews
Chemical Reviews is peer-reviewed scientific journal published twice per month by the American Chemical Society.
New!!: (E)-Stilbene and Chemical Reviews · See more »
Chemische Berichte
Chemische Berichte (usually abbreviated as Ber. or Chem. Ber.) was a German-language scientific journal of all disciplines of chemistry founded in 1868.
New!!: (E)-Stilbene and Chemische Berichte · See more »
Chirality
Chirality is a property of asymmetry important in several branches of science.
New!!: (E)-Stilbene and Chirality · See more »
Cis–trans isomerism
Cis–trans isomerism, also known as geometric isomerism or configurational isomerism, is a term used in organic chemistry.
New!!: (E)-Stilbene and Cis–trans isomerism · See more »
Conjugated system
In chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in molecules which are conventionally represented as having alternating single and multiple bonds, which in general may lower the overall energy of the molecule and increase stability.
New!!: (E)-Stilbene and Conjugated system · See more »
David Van Nostrand
David Van Nostrand (December 5, 1811, New York City – June 14, 1886, New York City) was a New York City publisher.
New!!: (E)-Stilbene and David Van Nostrand · See more »
Derivative (chemistry)
In chemistry, a derivative is a compound that is derived from a similar compound by a chemical reaction.
New!!: (E)-Stilbene and Derivative (chemistry) · See more »
Diarylethene
In chemistry, diarylethene is the general name of a class of compounds that have aromatic groups bonded to each end of a carbon–carbon double bond.
New!!: (E)-Stilbene and Diarylethene · See more »
Dienestrol
Dienestrol (brand names Ortho Dienestrol, Dienoestrol, Dienoestrol Ortho, Sexadien, Denestrolin, Dienol, Dinovex, Follormon, Oestrodiene, Synestrol, numerous others), also known as dienoestrol, is a synthetic nonsteroidal estrogen of the stilbestrol group which is or was used to treat menopausal symptoms in the United States and Europe.
New!!: (E)-Stilbene and Dienestrol · See more »
Diethylstilbestrol
Diethylstilbestrol (DES), also known as stilbestrol or stilboestrol, is an estrogen medication which is mostly no longer used.
New!!: (E)-Stilbene and Diethylstilbestrol · See more »
Diol
A diol or glycol is a chemical compound containing two hydroxyl groups (−OH groups).
New!!: (E)-Stilbene and Diol · See more »
Disodium 4,4'-dinitrostilbene-2,2'-disulfonate
Disodium 4,4′-dinitrostilbene-2,2′-disulfonate is an organic compound with the formula (O2NC6H3(SO3Na)CH)2 This salt is a common precursor to a variety of textile dyes.
New!!: (E)-Stilbene and Disodium 4,4'-dinitrostilbene-2,2'-disulfonate · See more »
Double bond
A double bond in chemistry is a chemical bond between two chemical elements involving four bonding electrons instead of the usual two.
New!!: (E)-Stilbene and Double bond · See more »
Dye
A dye is a colored substance that has an affinity to the substrate to which it is being applied.
New!!: (E)-Stilbene and Dye · See more »
Dye laser
A dye laser is a laser which uses an organic dye as the lasing medium, usually as a liquid solution.
New!!: (E)-Stilbene and Dye laser · See more »
E-Z notation
E-Z configuration, or the E-Z convention, is the IUPAC preferred method of describing the absolute stereochemistry of double bonds in organic chemistry.
New!!: (E)-Stilbene and E-Z notation · See more »
Elsevier
Elsevier is an information and analytics company and one of the world's major providers of scientific, technical, and medical information.
New!!: (E)-Stilbene and Elsevier · See more »
Enantiomer
In chemistry, an enantiomer, also known as an optical isomer (and archaically termed antipode or optical antipode), is one of two stereoisomers that are mirror images of each other that are non-superposable (not identical), much as one's left and right hands are the same except for being reversed along one axis (the hands cannot be made to appear identical simply by reorientation).
New!!: (E)-Stilbene and Enantiomer · See more »
Enantiomeric excess
Enantiomeric excess (ee) is a measurement of purity used for chiral substances.
New!!: (E)-Stilbene and Enantiomeric excess · See more »
Epoxide
An epoxide is a cyclic ether with a three-atom ring.
New!!: (E)-Stilbene and Epoxide · See more »
Estrogen
Estrogen, or oestrogen, is the primary female sex hormone.
New!!: (E)-Stilbene and Estrogen · See more »
Ethylene
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula or H2C.
New!!: (E)-Stilbene and Ethylene · See more »
Ethylene oxide
Ethylene oxide, called oxirane by IUPAC, is an organic compound with the formula. It is a cyclic ether and the simplest epoxide: a three-membered ring consisting of one oxygen atom and two carbon atoms. Ethylene oxide is a colorless and flammable gas with a faintly sweet odor. Because it is a strained ring, ethylene oxide easily participates in a number of addition reactions that result in ring-opening. Ethylene oxide is isomeric with acetaldehyde and with vinyl alcohol. Ethylene oxide is industrially produced by oxidation of ethylene in the presence of silver catalyst. The reactivity that is responsible for many of ethylene oxide's hazards also make it useful. Although too dangerous for direct household use and generally unfamiliar to consumers, ethylene oxide is used for making many consumer products as well as non-consumer chemicals and intermediates. These products include detergents, thickeners, solvents, plastics, and various organic chemicals such as ethylene glycol, ethanolamines, simple and complex glycols, polyglycol ethers, and other compounds. Although it is a vital raw material with diverse applications, including the manufacture of products like polysorbate 20 and polyethylene glycol (PEG) that are often more effective and less toxic than alternative materials, ethylene oxide itself is a very hazardous substance. At room temperature it is a flammable, carcinogenic, mutagenic, irritating, and anaesthetic gas. As a toxic gas that leaves no residue on items it contacts, ethylene oxide is a surface disinfectant that is widely used in hospitals and the medical equipment industry to replace steam in the sterilization of heat-sensitive tools and equipment, such as disposable plastic syringes. It is so flammable and extremely explosive that it is used as a main component of thermobaric weapons; therefore, it is commonly handled and shipped as a refrigerated liquid to control its hazardous nature.Rebsdat, Siegfried and Mayer, Dieter (2005) "Ethylene Oxide" in Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH, Weinheim..
New!!: (E)-Stilbene and Ethylene oxide · See more »
Fosfestrol
Fosfestrol (brand names Honvan, Difostilben, Fosfostilben, Fostrolin, Stilbol, Stilphostrol, Vagestrol, among others), also known as diethylstilbestrol diphosphate, abbreviated as DESDP or DESP, is a synthetic nonsteroidal estrogen of the stilbestrol group which is or has been used in the treatment of prostate cancer.
New!!: (E)-Stilbene and Fosfestrol · See more »
Greek language
Greek (Modern Greek: ελληνικά, elliniká, "Greek", ελληνική γλώσσα, ellinikí glóssa, "Greek language") is an independent branch of the Indo-European family of languages, native to Greece and other parts of the Eastern Mediterranean and the Black Sea.
New!!: (E)-Stilbene and Greek language · See more »
Halogen addition reaction
A halogen addition reaction is a simple organic reaction where a halogen molecule is added to the carbon–carbon double bond of an alkene functional group.
New!!: (E)-Stilbene and Halogen addition reaction · See more »
Halonium ion
A halonium ion in organic chemistry is any onium compound (ion) containing a halogen atom carrying a positive charge.
New!!: (E)-Stilbene and Halonium ion · See more »
Heck reaction
The Heck reaction (also called the Mizoroki-Heck reaction) is the chemical reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst (or palladium nanomaterial-based catalyst) to form a substituted alkene.
New!!: (E)-Stilbene and Heck reaction · See more »
Inorganic Chemistry (journal)
Inorganic Chemistry is a biweekly peer-reviewed scientific journal published by the American Chemical Society since 1962.
New!!: (E)-Stilbene and Inorganic Chemistry (journal) · See more »
Iodobenzene
Iodobenzene is an organoiodine compound consisting of a benzene ring substituted with one iodine atom.
New!!: (E)-Stilbene and Iodobenzene · See more »
Journal of Chemical Physics
The Journal of Chemical Physics is a scientific journal published by the American Institute of Physics that carries research papers on chemical physics.
New!!: (E)-Stilbene and Journal of Chemical Physics · See more »
Journal of Organic Chemistry
The Journal of Organic Chemistry, colloquially known as JOC or J Org, is a peer-reviewed scientific journal for original contributions of fundamental research in all branches of theory and practice in organic and bioorganic chemistry.
New!!: (E)-Stilbene and Journal of Organic Chemistry · See more »
Journal of the American Chemical Society
The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.
New!!: (E)-Stilbene and Journal of the American Chemical Society · See more »
Karl Barry Sharpless
Karl Barry Sharpless (born April 28, 1941) is an American chemist known for his work on stereoselective reactions.
New!!: (E)-Stilbene and Karl Barry Sharpless · See more »
Lemieux–Johnson oxidation
The Lemieux–Johnson or Malaprade–Lemieux–Johnson oxidation is a chemical reaction in which an olefin undergoes oxidative cleavage to form two aldehyde or ketone units.
New!!: (E)-Stilbene and Lemieux–Johnson oxidation · See more »
Mechanistic organic photochemistry
Mechanistic organic photochemistry is that aspect of organic photochemistry which seeks to explain the mechanisms of organic photochemical reactions.
New!!: (E)-Stilbene and Mechanistic organic photochemistry · See more »
Meso compound
A meso compound or meso isomer is a stereoisomer with an identical or superimposable mirror image i.e., a non-optically active member of a set of stereoisomers, at least two of which are optically active.
New!!: (E)-Stilbene and Meso compound · See more »
Moiety (chemistry)
In organic chemistry, a moiety is a part of a molecule.
New!!: (E)-Stilbene and Moiety (chemistry) · See more »
Nitromethane
Nitromethane is an organic compound with the chemical formula.
New!!: (E)-Stilbene and Nitromethane · See more »
Novartis
Novartis International AG is a Swiss multinational pharmaceutical company based in Basel, Switzerland.
New!!: (E)-Stilbene and Novartis · See more »
Optical brightener
Optical brighteners, optical brightening agents (OBAs), fluorescent brightening agents (FBAs), or fluorescent whitening agents (FWAs), are chemical compounds that absorb light in the ultraviolet and violet region (usually 340-370 nm) of the electromagnetic spectrum, and re-emit light in the blue region (typically 420-470 nm) by fluorescence.
New!!: (E)-Stilbene and Optical brightener · See more »
Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
New!!: (E)-Stilbene and Organic compound · See more »
Organic Reactions
Organic Reactions is a secondary reference which synthesizes the organic chemistry literature around particular chemical transformations.
New!!: (E)-Stilbene and Organic Reactions · See more »
Ozonolysis
Ozonolysis is an organic reaction where the unsaturated bonds of alkenes, alkynes, or azo compounds are cleaved with ozone.
New!!: (E)-Stilbene and Ozonolysis · See more »
Phenanthrene
Phenanthrene is a polycyclic aromatic hydrocarbon composed of three fused benzene rings.
New!!: (E)-Stilbene and Phenanthrene · See more »
Phenyl group
In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.
New!!: (E)-Stilbene and Phenyl group · See more »
Phosphor
A phosphor, most generally, is a substance that exhibits the phenomenon of luminescence.
New!!: (E)-Stilbene and Phosphor · See more »
Photochemistry
Photochemistry is the branch of chemistry concerned with the chemical effects of light.
New!!: (E)-Stilbene and Photochemistry · See more »
Potassium permanganate
Potassium permanganate is an inorganic chemical compound and medication.
New!!: (E)-Stilbene and Potassium permanganate · See more »
Pterostilbene
Pterostilbene is a stilbenoid chemically related to resveratrol.
New!!: (E)-Stilbene and Pterostilbene · See more »
Racemic mixture
In chemistry, a racemic mixture, or racemate, is one that has equal amounts of left- and right-handed enantiomers of a chiral molecule.
New!!: (E)-Stilbene and Racemic mixture · See more »
Relative permittivity
The relative permittivity of a material is its (absolute) permittivity expressed as a ratio relative to the permittivity of vacuum.
New!!: (E)-Stilbene and Relative permittivity · See more »
Resveratrol
Resveratrol (3,5,4′-trihydroxy-trans-stilbene) is a stilbenoid, a type of natural phenol, and a phytoalexin produced by several plants in response to injury or, when the plant is under attack by pathogens such as bacteria or fungi.
New!!: (E)-Stilbene and Resveratrol · See more »
Richard F. Heck
Richard Frederick Heck (August 15, 1931 – October 10, 2015) was an American chemist noted for the discovery and development of the Heck reaction, which uses palladium to catalyze organic chemical reactions that couple aryl halides with alkenes.
New!!: (E)-Stilbene and Richard F. Heck · See more »
Scintillator
A scintillator is a material that exhibits scintillation—the property of luminescence, when excited by ionizing radiation.
New!!: (E)-Stilbene and Scintillator · See more »
Sharpless asymmetric dihydroxylation
Sharpless asymmetric dihydroxylation (also called the Sharpless bishydroxylation) is the chemical reaction of an alkene with osmium tetroxide in the presence of a chiral quinine ligand to form a vicinal diol.
New!!: (E)-Stilbene and Sharpless asymmetric dihydroxylation · See more »
Sodium hypochlorite
No description.
New!!: (E)-Stilbene and Sodium hypochlorite · See more »
Springer Science+Business Media
Springer Science+Business Media or Springer, part of Springer Nature since 2015, is a global publishing company that publishes books, e-books and peer-reviewed journals in science, humanities, technical and medical (STM) publishing.
New!!: (E)-Stilbene and Springer Science+Business Media · See more »
Stereoisomerism
In stereochemistry, stereoisomers are isomeric molecules that have the same molecular formula and sequence of bonded atoms (constitution), but differ in the three-dimensional orientations of their atoms in space.
New!!: (E)-Stilbene and Stereoisomerism · See more »
Steric effects
Steric effects are nonbonding interactions that influence the shape (conformation) and reactivity of ions and molecules.
New!!: (E)-Stilbene and Steric effects · See more »
Stilbenoid
Stilbenoids are hydroxylated derivatives of stilbene.
New!!: (E)-Stilbene and Stilbenoid · See more »
Stilbestrol
Stilbestrol, or stilboestrol, also known as 4,4'-dihydroxystilbene or 4,4'-stilbenediol, is a stilbenoid and the parent compound of a group of nonsteroidal estrogens that includes, most notably, diethylstilbestrol.
New!!: (E)-Stilbene and Stilbestrol · See more »
Structural formula
The structural formula of a chemical compound is a graphic representation of the molecular structure, showing how the atoms are arranged.
New!!: (E)-Stilbene and Structural formula · See more »
Styrene
Styrene, also known as ethenylbenzene, vinylbenzene, and phenylethene, is an organic compound with the chemical formula C6H5CH.
New!!: (E)-Stilbene and Styrene · See more »
Substituent
In organic chemistry and biochemistry, a substituent is an atom or group of atoms which replaces one or more hydrogen atoms on the parent chain of a hydrocarbon, becoming a moiety of the resultant new molecule.
New!!: (E)-Stilbene and Substituent · See more »
Tert-Butyl hydroperoxide
tert-Butyl hydroperoxide (tBuOOH) is an organic peroxide widely used in a variety of oxidation processes, for example Sharpless epoxidation.
New!!: (E)-Stilbene and Tert-Butyl hydroperoxide · See more »
Tetrahedron Letters
Tetrahedron Letters is a weekly international journal for rapid publication of full original research papers in the field of organic chemistry.
New!!: (E)-Stilbene and Tetrahedron Letters · See more »
Ullmann's Encyclopedia of Industrial Chemistry
Ullmann's Encyclopedia of Industrial Chemistry is a reference work related to industrial chemistry published in English and German.
New!!: (E)-Stilbene and Ullmann's Encyclopedia of Industrial Chemistry · See more »
Upjohn dihydroxylation
The Upjohn dihydroxylation is an organic reaction which converts an alkene to a cis vicinal diol.
New!!: (E)-Stilbene and Upjohn dihydroxylation · See more »
Vicinal (chemistry)
In chemistry the descriptor vicinal (from Latin vicinus.
New!!: (E)-Stilbene and Vicinal (chemistry) · See more »
Wiley-VCH
Wiley-VCH is a German publisher owned by John Wiley & Sons.
New!!: (E)-Stilbene and Wiley-VCH · See more »
(Z)-Stilbene
(Z)-Stilbene is a diarylethene, that is, a hydrocarbon consisting of a cis ethene double bond substituted with a phenyl group on both carbon atoms of the double bond.
New!!: (E)-Stilbene and (Z)-Stilbene · See more »
1,4-Dioxane
1,4-Dioxane is a heterocyclic organic compound, classified as an ether.
New!!: (E)-Stilbene and 1,4-Dioxane · See more »
4-Nitrotoluene
4-Nitrotoluene or para-nitrotoluene is an organic compound with the formula CH3C6H4NO2.
New!!: (E)-Stilbene and 4-Nitrotoluene · See more »
Redirects here:
References
[1] https://en.wikipedia.org/wiki/(E)-Stilbene
