Hydrocarbons
Halides
Organic Fluorine Compounds
Aromatic Compounds
Heterocyclic Compounds
Alcohols, Phenols and Ethers
Aldehydes, Ketones and Quinones
Carboxylic Acids and Derivatives
Esters
Nitrogen Compounds
Nitriles
Organometallic Compounds
Organometalate
Carbohydrate
Amino Acids, Proteins and Nucleic Acids
Organo Silicon Compounds
CAS:4165-57-5
Molecular Formula:C6BrD5
Alias
More Information
1-Bromopentadeuteriobenzene; 1-Bromopentadeuterobenzene; Benzene-d5,Bromo; Pentadeuterobromobenzene; Einecs 224-013-8; Ammonium-d4 Chloride; Bromobenzene-D5; d5-Phenyl Bromide; Bromobenzene-D5-D; Bromo(2H5)Benzene
Brief Introduction
The labelled version of Bromobenzene, used as a general reagent in palladium-catalyzed reactions and in the synthesis of Grignard reagents.
CAS:425-61-6
Molecular Formula:C4H6F4O2
Alias
More Information
2,2,3,3-Tetrafluorobutane-1,4-diol; 1h,1h,4h,4h-Perfluoro-1,4-Butanediol; 1,4-Dihydroxy-2,2,3,3-Tetrafluorobutane
CAS:51-44-5
Molecular Formula:C7H4Cl2O2
Alias
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Dichlorobenzoic Acid
Brief Introduction
3,4-dichlorobenzoic acid is a chlorobenzoic acid carrying chloro substituents at positions 3 and 4. It is a conjugate acid of a 3,4-dichlorobenzoate.
CAS:55362-80-6
Molecular Formula:C9H19BrO
Alias
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9-Bromononan-1-ol; 1-Nonanol, 9-Bromo-; 9-Bromo-Nonan-1-ol
Brief Introduction
9-bromo-1-nonanol is an organic intermediate, which can be obtained from 1,9-nonanediol after bromination. It is reported that it can be used to prepare sex pheromone of Spodoptera litura.
CAS:555-60-2
Molecular Formula:C9H5ClN4
Alias
More Information
CCCP; Carbonyl Cyanide 3-Chlorophenylhydrazone; Carbonyl Cyanide m-Chlorophenylhydrazone; Carbonylcyanide-3-Chlorophenylhydrazone; Carbonyl Cyanide m-Chlorophenyl Hydrazone; m-Chlorophenyl Carbonylcyanide Hydrazone; [(3-Chlorophenyl)Hydrazono]Malononitrile; (3-Chlorophenyl)Carbonohydrazonoyl Dicyanide; Propanedinitrile, [(3-Chlorophenyl)Hydrazono]-; Mesoxalonitrile, (m-Chlorophenyl)Hydrazone; Propanedinitrile, ((3-Chlorophenyl)Hydrazono)-; ((3-Chlorophenyl)Hydrazono)Propanedinitrile; Carbonyl Cyanide, (3-Chlorophenyl)Hydrazone; Carbonyl Cyanide Chlorophenylhydrazone; Carbonylcyanide-m-Chlorophenylhydrazone; Carbonyl Cyanide-m-Chlorophenylhydrazone; 2-[(3-Chlorophenyl)Hydrazinylidene]Propanedinitrile; ((3-Chlorophenyl)Hydrazono)Malononitrile; Carbonyl Cyanide (m-Chlorophenyl)Hydrazone; Carbonylcyanide m-Chlorophenylhydrazone; Carbonyl Cyanide, 3-Chlorophenylhydrazone; [(3-Chlorophenyl)Hydrazono]Propanedinitrile; N'-(3-Chlorophenyl)Carbonohydrazonoyl Dicyanide; Propanedinitrile, 2-(2-(3-Chlorophenyl)Hydrazinylidene)-; Carbonyl Cyanide 3-Chlorophenylhydrazone;Carbonyl Cyanide m-Chlorophenylhydrazone; 2-((3-Chlorophenyl)Hydrazono)Malononitrile; 2-[(3-Chlorophenyl)Hydrazono]Malononitrile; Mesoxalonitrile 3-Chlorophenylhydrazone; Propanedinitrile, 2-[2-(3-Chlorophenyl)Hydrazinylidene]-; 2-[(3-Chlorophenyl)-Hydrazono]Malononitrile; Carbonylcyanide3-Chlorophenylhydrazone; (3-Chlorophenyl)Carbonohydrazonoyldicyanide; 2-[(3-Chlorophenyl)Hydrazono]Propanedinitrile; 3-Chlorophenylhydrazonopropanedinitrile; N-(3-Chlorophenyl)Carbonohydrazonoyl Dicyanide; Carbonyl Cyanide (3-Chlorophenyl)Hydrazone; [2-(3-Chlorophenyl)Hydrazinylidene]Propanedinitrile; N-(3-Chlorophenyl)-1-Cyanomethanecarbohydrazonoyl Cyanide
Brief Introduction
It is an inhibitor of Oxidative phosphorylation. It is an ion carrier. Generally speaking, CCCP leads to gradual cell damage and the death of living organisms. It mainly affects protein synthesis in mitochondria. The mechanism of CCCP is to decouple the proton concentration gradient formed by the normal activity of the Electron transport chain. This chemical substance essentially reduces the ability of ATP synthase to operate optimally in the form of ion carriers.
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