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・ 2,4-Diacetylphloroglucinol
・ 2,4-diaminopentanoate dehydrogenase
・ 2,4-Diaminopyrimidine
・ 2,4-Diaminotoluene
・ 2,4-dichlorobenzoyl-CoA reductase
・ 2,4-Dichlorobenzyl alcohol
・ 2,4-Dichlorophenol
・ 2,4-dichlorophenol 6-monooxygenase
・ 2,4-Dichlorophenoxyacetic acid
・ 2,4-Dihydroxy-1,4-benzoxazin-3-one-glucoside dioxygenase
・ 2,4-Dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2 -D-glucosyltransferase
・ 2,4-Dihydroxybenzoic acid
・ 2,4-Dimethoxybenzaldehyde
・ 2,4-Dimethyl-6-tert-butylphenol
・ 2,4-Dinitroanisole
2,4-Dinitrochlorobenzene
・ 2,4-Dinitrophenol
・ 2,4-Dinitrophenylhydrazine
・ 2,4-Dinitrophenylmorphine
・ 2,4-Dinitrotoluene
・ 2,4-Dithiapentane
・ 2,4-DNP
・ 2,4-Xylidine
・ 2,5-Bis(hydroxymethyl)furan
・ 2,5-diamino-6-(ribosylamino)-4(3H)-pyrimidinone 5'-phosphate reductase
・ 2,5-Diamino-6-hydroxy-4-(5-phosphoribosylamino)pyrimidine
・ 2,5-Diaminotoluene
・ 2,5-diaminovalerate transaminase
・ 2,5-Dichloroaniline
・ 2,5-didehydrogluconate reductase


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2,4-Dinitrochlorobenzene : ウィキペディア英語版
2,4-Dinitrochlorobenzene

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2,4-Dinitrochlorobenzene (DNCB) is an organic compound with the formula (O2N)2C6H3Cl. It is a yellow solid that is soluble in organic solvents. It is an important intermediate for the industrial production of other compounds.〔Gerald Booth (2007). "Nitro Compounds, Aromatic". In: ''Ullmann's Encyclopedia of Industrial Chemistry''. John Wiley & Sons: New York. 〕
DNCB is produced commercially by the nitration of p-nitrochlorobenzene with a mixture of nitric and sulfuric acids. Other methods afford the compound less efficiently include the chlorination of dinitrobenzene, nitration of o-nitrochlorobenzene and the dinitration of chlorobenzene.
==Uses==
By virtue of the two nitro groups, the chloride is susceptible to nucleophilic substitution. In this way, the compound is a precursor to many other compounds. Base gives the dinitrophenol, ammonia the dinitroaniline, methoxide the dinitroanisole, and amines the secondary amines.

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