Amino Acids, Proteins and Nucleic Acids
Alcohols, Phenols and Ethers
Organo Silicon Compounds
Halides
Heterocyclic Compounds
Organic Fluorine Compounds
Nitrogen Compounds
Organometallic Compounds
Esters
Hydrocarbons
Aromatic Compounds
Carboxylic Acids and Derivatives
Nitriles
Organometalate
Aldehydes, Ketones and Quinones
Carbohydrate
CAS:425-61-6
Molecular Formula:C4H6F4O2
Alias
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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:450-93-1
Molecular Formula:C7H7FO2
Alias
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2-Methoxy-4-Fluorophenol; 4-Fluoroguaiacol, 5-Fluoro-2-Hydroxyanisole; 4-Fluoro-2-Methyoxyphenol; 4-Fluoroguaiacol
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
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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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