Table of Contents
79 relations: Alcohol (chemistry), Aldehyde, Alkyl group, Amide, Amine, Annales de chimie et de physique, Antihistamine, Antihypertensive drug, Archiv der Pharmazie, Arene substitution pattern, Aryl group, Azelastine, Beilstein Journal of Organic Chemistry, Benzaldehyde, Benzene, Benzodiazepine, Bromine, Building block (chemistry), Butyllithium, Carbonylation, Carboxylic acid, Chemical compound, Chemistry: A European Journal, Cinchonine, Condensation reaction, Cross-coupling reaction, Diethyl ether, Dimethyl sulfoxide, Dimethylphosphite, Disodium tetracarbonylferrate, Enantiomeric excess, Ethanol, European Journal of Organic Chemistry, Fine chemical, Glycerol, Grignard reagent, Halogenation, Helvetica Chimica Acta, Heterocyclic compound, Horner–Wadsworth–Emmons reaction, Hydralazine, Hydrazine, Iron(III) chloride, Isocoumarin, Isocyanide, Journal of the American Chemical Society, Lactol, Liebigs Annalen, Montmorillonite, Morpholine, ... Expand index (29 more) »
- Aldehydic acids
- Benzaldehydes
Alcohol (chemistry)
In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group bound to carbon.
See 2-Carboxybenzaldehyde and Alcohol (chemistry)
Aldehyde
In organic chemistry, an aldehyde is an organic compound containing a functional group with the structure.
See 2-Carboxybenzaldehyde and Aldehyde
Alkyl group
In organic chemistry, an alkyl group is an alkane missing one hydrogen.
See 2-Carboxybenzaldehyde and Alkyl group
Amide
In organic chemistry, an amide, also known as an organic amide or a carboxamide, is a compound with the general formula, where R, R', and R″ represent any group, typically organyl groups or hydrogen atoms.
See 2-Carboxybenzaldehyde and Amide
Amine
In chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.
See 2-Carboxybenzaldehyde and Amine
Annales de chimie et de physique
Annales de chimie et de physique (French for Annals of Chemistry and Physics) is a scientific journal founded in Paris, France, in 1789 under the title Annales de chimie.
See 2-Carboxybenzaldehyde and Annales de chimie et de physique
Antihistamine
Antihistamines are drugs which treat allergic rhinitis, common cold, influenza, and other allergies.
See 2-Carboxybenzaldehyde and Antihistamine
Antihypertensive drug
Antihypertensives are a class of drugs that are used to treat hypertension (high blood pressure).
See 2-Carboxybenzaldehyde and Antihypertensive drug
Archiv der Pharmazie
The Archiv der Pharmazie (German pronunciation:, English: Archive of Pharmacy) is a monthly peer-reviewed scientific journal covering all aspects of chemistry in the life sciences.
See 2-Carboxybenzaldehyde and Archiv der Pharmazie
Arene substitution pattern
Arene substitution patterns are part of organic chemistry IUPAC nomenclature and pinpoint the position of substituents other than hydrogen in relation to each other on an aromatic hydrocarbon.
See 2-Carboxybenzaldehyde and Arene substitution pattern
Aryl group
In organic chemistry, an aryl is any functional group or substituent derived from an aromatic ring, usually an aromatic hydrocarbon, such as phenyl and naphthyl.
See 2-Carboxybenzaldehyde and Aryl group
Azelastine
Azelastine, sold under the brand name Astelin among others, is a H1 receptor-blocking medication primarily used as a nasal spray to treat allergic rhinitis (hay fever) and as eye drops for allergic conjunctivitis.
See 2-Carboxybenzaldehyde and Azelastine
Beilstein Journal of Organic Chemistry
The Beilstein Journal of Organic Chemistry is a peer-reviewed open-access scientific journal established in 2005.
See 2-Carboxybenzaldehyde and Beilstein Journal of Organic Chemistry
Benzaldehyde
Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent. 2-Carboxybenzaldehyde and Benzaldehyde are Benzaldehydes.
See 2-Carboxybenzaldehyde and Benzaldehyde
Benzene
Benzene is an organic chemical compound with the molecular formula C6H6. The benzene molecule is composed of six carbon atoms joined in a planar hexagonal ring with one hydrogen atom attached to each. Because it contains only carbon and hydrogen atoms, benzene is classed as a hydrocarbon. Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals.
See 2-Carboxybenzaldehyde and Benzene
Benzodiazepine
Benzodiazepines (BZD, BDZ, BZs), colloquially called "benzos", are a class of depressant drugs whose core chemical structure is the fusion of a benzene ring and a diazepine ring.
See 2-Carboxybenzaldehyde and Benzodiazepine
Bromine
Bromine is a chemical element; it has symbol Br and atomic number 35.
See 2-Carboxybenzaldehyde and Bromine
Building block (chemistry)
Building block is a term in chemistry which is used to describe a virtual molecular fragment or a real chemical compound the molecules of which possess reactive functional groups.
See 2-Carboxybenzaldehyde and Building block (chemistry)
Butyllithium
Butyllithium may refer to one of 5 isomeric organolithium reagents of which 3 are commonly used in chemical synthesis.
See 2-Carboxybenzaldehyde and Butyllithium
Carbonylation
In chemistry, carbonylation refers to reactions that introduce carbon monoxide (CO) into organic and inorganic substrates.
See 2-Carboxybenzaldehyde and Carbonylation
Carboxylic acid
In organic chemistry, a carboxylic acid is an organic acid that contains a carboxyl group attached to an R-group.
See 2-Carboxybenzaldehyde and Carboxylic acid
Chemical compound
A chemical compound is a chemical substance composed of many identical molecules (or molecular entities) containing atoms from more than one chemical element held together by chemical bonds.
See 2-Carboxybenzaldehyde and Chemical compound
Chemistry: A European Journal
Chemistry: A European Journal is a weekly peer-reviewed scientific journal that covers all areas of chemistry and related fields.
See 2-Carboxybenzaldehyde and Chemistry: A European Journal
Cinchonine
Cinchonine is an alkaloid found in Cinchona officinalis.
See 2-Carboxybenzaldehyde and Cinchonine
Condensation reaction
In organic chemistry, a condensation reaction is a type of chemical reaction in which two molecules are combined to form a single molecule, usually with the loss of a small molecule such as water.
See 2-Carboxybenzaldehyde and Condensation reaction
Cross-coupling reaction
In organic chemistry, a cross-coupling reaction is a reaction where two different fragments are joined.
See 2-Carboxybenzaldehyde and Cross-coupling reaction
Diethyl ether
Diethyl ether, or simply ether, is an organic compound with the chemical formula, sometimes abbreviated as.
See 2-Carboxybenzaldehyde and Diethyl ether
Dimethyl sulfoxide
Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2.
See 2-Carboxybenzaldehyde and Dimethyl sulfoxide
Dimethylphosphite
Dimethylphosphite is an organophosphorus compound with the formula (CH3O)2P(O)H, known as dimethyl hydrogen phosphite (DMHP).
See 2-Carboxybenzaldehyde and Dimethylphosphite
Disodium tetracarbonylferrate
Disodium tetracarbonylferrate is the organoiron compound with the formula Na2.
See 2-Carboxybenzaldehyde and Disodium tetracarbonylferrate
Enantiomeric excess
In stereochemistry, enantiomeric excess (ee) is a measurement of purity used for chiral substances.
See 2-Carboxybenzaldehyde and Enantiomeric excess
Ethanol
Ethanol (also called ethyl alcohol, grain alcohol, drinking alcohol, or simply alcohol) is an organic compound with the chemical formula.
See 2-Carboxybenzaldehyde and Ethanol
European Journal of Organic Chemistry
The European Journal of Organic Chemistry is a weekly peer-reviewed scientific journal covering organic chemistry.
See 2-Carboxybenzaldehyde and European Journal of Organic Chemistry
Fine chemical
In chemistry, fine chemicals are complex, single, pure chemical substances, produced in limited quantities in multipurpose plants by multistep batch chemical or biotechnological processes.
See 2-Carboxybenzaldehyde and Fine chemical
Glycerol
Glycerol, also called glycerine or glycerin, is a simple triol compound.
See 2-Carboxybenzaldehyde and Glycerol
Grignard reagent
Grignard reagents or Grignard compounds are chemical compounds with the general formula, where X is a halogen and R is an organic group, normally an alkyl or aryl.
See 2-Carboxybenzaldehyde and Grignard reagent
Halogenation
In chemistry, halogenation is a chemical reaction which introduces one or more halogens into a chemical compound.
See 2-Carboxybenzaldehyde and Halogenation
Helvetica Chimica Acta
Helvetica Chimica Acta is a peer-reviewed scientific journal of chemistry established by the Swiss Chemical Society.
See 2-Carboxybenzaldehyde and Helvetica Chimica Acta
Heterocyclic compound
A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s).
See 2-Carboxybenzaldehyde and Heterocyclic compound
Horner–Wadsworth–Emmons reaction
The Horner–Wadsworth–Emmons (HWE) reaction is a chemical reaction used in organic chemistry of stabilized phosphonate carbanions with aldehydes (or ketones) to produce predominantly E-alkenes.
See 2-Carboxybenzaldehyde and Horner–Wadsworth–Emmons reaction
Hydralazine
Hydralazine, sold under the brand name Apresoline among others, is a medication used to treat high blood pressure and heart failure.
See 2-Carboxybenzaldehyde and Hydralazine
Hydrazine
Hydrazine is an inorganic compound with the chemical formula.
See 2-Carboxybenzaldehyde and Hydrazine
Iron(III) chloride
Iron(III) chloride describes the inorganic compounds with the formula (H2O)x.
See 2-Carboxybenzaldehyde and Iron(III) chloride
Isocoumarin
Isocoumarin (1H-2-benzopyran-1-one; 3,4-benzo-2-pyrone) is a lactone, a type of natural organic compound.
See 2-Carboxybenzaldehyde and Isocoumarin
Isocyanide
An isocyanide (also called isonitrile or carbylamine) is an organic compound with the functional group –.
See 2-Carboxybenzaldehyde and Isocyanide
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.
See 2-Carboxybenzaldehyde and Journal of the American Chemical Society
Lactol
In organic chemistry, a lactol is a functional group which is the cyclic equivalent of a hemiacetal or a hemiketal.
See 2-Carboxybenzaldehyde and Lactol
Liebigs Annalen
Justus Liebig's Annalen der Chemie (often cited as Liebigs Annalen) was one of the oldest and historically most important journals in the field of organic chemistry worldwide.
See 2-Carboxybenzaldehyde and Liebigs Annalen
Montmorillonite
Montmorillonite is a very soft phyllosilicate group of minerals that form when they precipitate from water solution as microscopic crystals, known as clay.
See 2-Carboxybenzaldehyde and Montmorillonite
Morpholine
Morpholine is an organic chemical compound having the chemical formula O(CH2CH2)2NH.
See 2-Carboxybenzaldehyde and Morpholine
Multi-component reaction
A multi-component reaction (or MCR), sometimes referred to as a "Multi-component Assembly Process" (or MCAP), is a chemical reaction where three or more compounds react to form a single product.
See 2-Carboxybenzaldehyde and Multi-component reaction
Nanowire
doi-access.
See 2-Carboxybenzaldehyde and Nanowire
Naphthalene
Naphthalene is an organic compound with formula.
See 2-Carboxybenzaldehyde and Naphthalene
Natural product
A natural product is a natural compound or substance produced by a living organism—that is, found in nature.
See 2-Carboxybenzaldehyde and Natural product
O-Xylene
o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C6H4(CH3)2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration).
See 2-Carboxybenzaldehyde and O-Xylene
Organic acid anhydride
An organic acid anhydride is an acid anhydride that is also an organic compound.
See 2-Carboxybenzaldehyde and Organic acid anhydride
Organic Letters
Organic Letters is a biweekly peer-reviewed scientific journal covering research in organic chemistry.
See 2-Carboxybenzaldehyde and Organic Letters
Ozone
Ozone (or trioxygen) is an inorganic molecule with the chemical formula.
See 2-Carboxybenzaldehyde and Ozone
P-Anisidine
p-Anisidine (or para-anisidine) is an organic compound with the formula CH3OC6H4NH2.
See 2-Carboxybenzaldehyde and P-Anisidine
Photochlorination
Photochlorination is a chlorination reaction that is initiated by light.
See 2-Carboxybenzaldehyde and Photochlorination
Phthalic anhydride
Phthalic anhydride is the organic compound with the formula C6H4(CO)2O.
See 2-Carboxybenzaldehyde and Phthalic anhydride
Phthalide
Phthalide is an organic chemical compound with the molecular formula C8H6O2.
See 2-Carboxybenzaldehyde and Phthalide
Potassium cyanide
Potassium cyanide is a compound with the formula KCN.
See 2-Carboxybenzaldehyde and Potassium cyanide
Potassium permanganate
Potassium permanganate is an inorganic compound with the chemical formula KMnO4.
See 2-Carboxybenzaldehyde and Potassium permanganate
Quinisocaine
Quinisocaine (INN) or dimethisoquin (BAN and USAN) is a topical anesthetic used as an antipruritic.
See 2-Carboxybenzaldehyde and Quinisocaine
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 or salt.
See 2-Carboxybenzaldehyde and Racemic mixture
Solvent
A solvent (from the Latin solvō, "loosen, untie, solve") is a substance that dissolves a solute, resulting in a solution.
See 2-Carboxybenzaldehyde and Solvent
Strecker amino acid synthesis
The Strecker amino acid synthesis, also known simply as the Strecker synthesis, is a method for the synthesis of amino acids by the reaction of an aldehyde with cyanide in the presence of ammonia.
See 2-Carboxybenzaldehyde and Strecker amino acid synthesis
Substituent
In organic chemistry, a substituent is one or a group of atoms that replaces (one or more) atoms, thereby becoming a moiety in the resultant (new) molecule.
See 2-Carboxybenzaldehyde and Substituent
Synthesis (journal)
Synthesis is a scientific journal published from 1969 to the present day by Thieme.
See 2-Carboxybenzaldehyde and Synthesis (journal)
Tautomer
Tautomers are structural isomers (constitutional isomers) of chemical compounds that readily interconvert.
See 2-Carboxybenzaldehyde and Tautomer
Tetrahedron (journal)
Tetrahedron is a weekly peer-reviewed scientific journal covering the field of organic chemistry.
See 2-Carboxybenzaldehyde and Tetrahedron (journal)
Tetrahedron Letters
Tetrahedron Letters is a weekly international journal for rapid publication of full original research papers in the field of organic chemistry.
See 2-Carboxybenzaldehyde and Tetrahedron Letters
The Journal of Organic Chemistry
The Journal of Organic Chemistry, colloquially known as JOC, is a peer-reviewed scientific journal for original contributions of fundamental research in all branches of theory and practice in organic and bioorganic chemistry.
See 2-Carboxybenzaldehyde and The Journal of Organic Chemistry
Thiol
In organic chemistry, a thiol, or thiol derivative, is any organosulfur compound of the form, where R represents an alkyl or other organic substituent.
See 2-Carboxybenzaldehyde and Thiol
Thionyl chloride
Thionyl chloride is an inorganic compound with the chemical formula.
See 2-Carboxybenzaldehyde and Thionyl chloride
Ugi reaction
In organic chemistry, the Ugi reaction is a multi-component reaction involving a ketone or aldehyde, an amine, an isocyanide and a carboxylic acid to form a bis-amide.
See 2-Carboxybenzaldehyde and Ugi reaction
Vasodilation
Vasodilation, also known as vasorelaxation, is the widening of blood vessels.
See 2-Carboxybenzaldehyde and Vasodilation
1,4-Dioxane
1,4-Dioxane is a heterocyclic organic compound, classified as an ether.
See 2-Carboxybenzaldehyde and 1,4-Dioxane
See also
Aldehydic acids
- 2-Aminomuconic semialdehyde
- 2-Carboxybenzaldehyde
- 2-Hydroxymuconate semialdehyde
- 4-Carboxybenzaldehyde
- Allysine
- Calostomal
- Elenolic acid
- Glutamate-5-semialdehyde
- Glyoxylic acid
- L-Aspartic-4-semialdehyde
- Methylmalonic acid semialdehyde
- Semialdehyde
- Succinic semialdehyde
- Tartronic acid semialdehyde
- Traumatin
Benzaldehydes
- 2,4-Dimethoxybenzaldehyde
- 2,5-Dimethoxybenzaldehyde
- 2-Aminobenzaldehyde
- 2-Carboxybenzaldehyde
- 2-Chloro-6-fluorobenzaldehyde
- 2-Chlorobenzaldehyde
- 2-Diphenylphosphinobenzaldehyde
- 2-Methoxybenzaldehyde
- 2-Methylbenzaldehyde
- 2-Nitrobenzaldehyde
- 3,4,5-Trimethoxybenzaldehyde
- 3-Acetyl-6-methoxybenzaldehyde
- 3-Bromobenzaldehyde
- 3-Nitrobenzaldehyde
- 4-Anisaldehyde
- 4-Bromobenzaldehyde
- 4-Carboxybenzaldehyde
- 4-Chlorobenzaldehyde
- 4-Ethylbenzaldehyde
- 4-Ethynylbenzaldehyde
- 4-Formylphenylboronic acid
- 4-Methylbenzaldehyde
- 4-Nitrobenzaldehyde
- AC-42
- Benzaldehyde
- Bromobenzaldehyde
- Casiraghi formylation
- Chlorobenzaldehyde
- Connorstictic acid
- Constictic acid
- Cuminaldehyde
- Dimethoxybenzaldehyde
- Flavipin
- Fluorobenzaldehyde
- Helicin
- Hericenone
- Hernandaline
- Isophthalaldehyde
- Mesitaldehyde
- Nemtabrutinib
- Nitrobenzaldehyde
- Para-Dimethylaminobenzaldehyde
- Phthalaldehyde
- Piperonal
- Taber's reagent
- Terephthalaldehyde
- Veratraldehyde
References
Also known as 2-Formylbenzoic acid.