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41 relations: Acetonitrile, Aluminium chloride, Barbituric acid, Beilstein Journal of Organic Chemistry, Benzaldehyde, Benzene, Catalysis, Chemical compound, Chlorine, Cis–trans isomerism, Diels–Alder reaction, Diethyl ether, Enol ether, Ethanol, Friedel–Crafts reaction, Gallium trichloride, Grignard reaction, Indium, Indium trihydride, Indium(III) bromide, Indium(III) fluoride, Knoevenagel condensation, Lewis acids and bases, Ligand, Lithium hydride, Methanol, Methyllithium, Monoclinic crystal system, Multi-component reaction, Octahedral molecular geometry, Organic reaction, Organic synthesis, Pearson symbol, Room temperature, Salt, Tetrahydrofuran, Thallium halides, Triethylindium, Trimethylindium, Yield (chemistry), Yttrium(III) chloride.
Acetonitrile
Acetonitrile is the chemical compound with the formula.
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Aluminium chloride
Aluminium chloride (AlCl3) is the main compound of aluminium and chlorine.
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Barbituric acid
Barbituric acid or malonylurea or 6-hydroxyuracil is an organic compound based on a pyrimidine heterocyclic skeleton.
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Beilstein Journal of Organic Chemistry
The Beilstein Journal of Organic Chemistry is a peer-reviewed open-access scientific journal established in 2005.
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Benzaldehyde
Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent.
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Benzene
Benzene is an important organic chemical compound with the chemical formula C6H6.
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Catalysis
Catalysis is the increase in the rate of a chemical reaction due to the participation of an additional substance called a catalysthttp://goldbook.iupac.org/C00876.html, which is not consumed in the catalyzed reaction and can continue to act repeatedly.
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Chemical compound
A chemical compound is a chemical substance composed of many identical molecules (or molecular entities) composed of atoms from more than one element held together by chemical bonds.
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Chlorine
Chlorine is a chemical element with symbol Cl and atomic number 17.
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Cis–trans isomerism
Cis–trans isomerism, also known as geometric isomerism or configurational isomerism, is a term used in organic chemistry.
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Diels–Alder reaction
The Diels–Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene derivative.
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Diethyl ether
Diethyl ether, or simply ether, is an organic compound in the ether class with the formula, sometimes abbreviated as (see Pseudoelement symbols).
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Enol ether
An enol ether is an alkene with an alkoxy substituent.
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Ethanol
Ethanol, also called alcohol, ethyl alcohol, grain alcohol, and drinking alcohol, is a chemical compound, a simple alcohol with the chemical formula.
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Friedel–Crafts reaction
The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring.
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Gallium trichloride
Gallium trichloride is the chemical compound with the formula GaCl3.
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Grignard reaction
The Grignard reaction (pronounced) is an organometallic chemical reaction in which alkyl, vinyl, or aryl-magnesium halides (Grignard reagents) add to a carbonyl group in an aldehyde or ketone.
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Indium
Indium is a chemical element with symbol In and atomic number 49.
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Indium trihydride
Indium trihydride is an inorganic compound with the chemical formulan (also written as (.
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Indium(III) bromide
Indium(III) bromide, (indium tribromide), InBr3, is a chemical compound of indium and bromine.
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Indium(III) fluoride
Indium(III) fluoride or indium trifluoride is the chemical compound composed of indium and fluorine with the formula InF3.
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Knoevenagel condensation
The Knoevenagel condensation reaction is an organic reaction named after Emil Knoevenagel.
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Lewis acids and bases
A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.
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Ligand
In coordination chemistry, a ligand is an ion or molecule (functional group) that binds to a central metal atom to form a coordination complex.
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Lithium hydride
Lithium hydride is an inorganic compound with the formula LiH.
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Methanol
Methanol, also known as methyl alcohol among others, is a chemical with the formula CH3OH (a methyl group linked to a hydroxyl group, often abbreviated MeOH).
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Methyllithium
Methyllithium is the simplest organolithium reagent with the empirical formula CH3Li.
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Monoclinic crystal system
In crystallography, the monoclinic crystal system is one of the 7 crystal systems.
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Multi-component reaction
In chemistry, 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.
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Octahedral molecular geometry
In chemistry, octahedral molecular geometry describes the shape of compounds with six atoms or groups of atoms or ligands symmetrically arranged around a central atom, defining the vertices of an octahedron.
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Organic reaction
Organic reactions are chemical reactions involving organic compounds.
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Organic synthesis
Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.
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Pearson symbol
The Pearson symbol, or Pearson notation, is used in crystallography as a means of describing a crystal structure, and was originated by W.B. Pearson.
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Room temperature
Colloquially, room temperature is the range of air temperatures that most people prefer for indoor settings, which feel comfortable when wearing typical indoor clothing.
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Salt
Salt, table salt or common salt is a mineral composed primarily of sodium chloride (NaCl), a chemical compound belonging to the larger class of salts; salt in its natural form as a crystalline mineral is known as rock salt or halite.
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Tetrahydrofuran
Tetrahydrofuran (THF) is an organic compound with the formula (CH2)4O.
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Thallium halides
The thallium halides include monohalides, where thallium has oxidation state +1, trihalides where thallium generally has oxidation state +3 and some intermediate halides with mixed +1 and +3 oxidation states.
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Triethylindium
Triethylindium is an olorganic chemical compound from the group of organometallic compounds.
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Trimethylindium
Trimethylindium (abbr: TMI or TMIn), In(CH3)3, (CAS #: 3385-78-2) is the preferred organometallic source of indium for metalorganic vapour phase epitaxy (MOVPE) of indium-containing compound semiconductors, such as InP, InAs, InN, InSb, GaInAs, InGaN, AlGaInP, AlInP, AlInGaNP, etc.
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Yield (chemistry)
In chemistry, yield, also referred to as reaction yield, is the amount of product obtained in a chemical reaction.
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Yttrium(III) chloride
Yttrium(III) chloride is an inorganic compound of yttrium and chloride.
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References
[1] https://en.wikipedia.org/wiki/Indium(III)_chloride
