192137-08-9

Basic information

• Product Name: Benzene, 1-(iodomethyl)-3,5-dinitro-
• CAS NO: 192137-08-9
• Molecular Formula: C7H5IN2O4
• Molecular Weight: 308.032
• Mol File: 192137-08-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(iodomethyl)-3,5-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(iodomethyl)-3,5-dinitro-(192137-08-9)
• EPA Substance Registry System: Benzene, 1-(iodomethyl)-3,5-dinitro-(192137-08-9)

Safety Data

• Hazardous Substances Data: 192137-08-9(Hazardous Substances Data)

Upstream product

• 74367-78-5 3,5-dinitrobenzyl chloride 
• 71022-43-0 3,5-dinitrobenzyl alcohol 
• 137570-75-3 1-bromomethyl-3,5-dinitrobenzene 

Downstream Products

• 252358-64-8 3-(3,5-dinitrobenzyl)-2-methyl-1,3-benzothiazol-3-ium iodide 
• 1453815-60-5 5-[(3,5-dinitrobenzyl)selanyl]-1-phenyl-1H-tetrazole 
• 1453815-61-6 N-(3,5-dinitrobenzyl)-N-phenylcyanamide 
• 1453815-62-7 (Z)-Se-(3,5-dinitrobenzyl)-N-cyano-N,N'-diphenylisoselenourea 
• 1453815-63-8 5-[(3,5-Dinitrobenzyl)selanyl]-1-(4-methoxyphenyl)-1H-tetrazole 
• 1453815-64-9 N-(3,5-dinitrobenzyl)-N-(4-methoxyphenyl)cyanamide 
• 1453815-65-0 (Z)-Se-(3,5-dinitrobenzyl)-N-cyano-N,N'-di(4-methoxyphenyl)isoselenourea 
• 1453815-66-1 1-(4-bromophenyl)-5-[(3,5-dinitrobenzyl)selanyl]-1H-tetrazole 
• 1453815-67-2 N-(4-Bromphenyl)-N-(3,5-dinitrobenzyl)cyanamide 
• 1453815-68-3 (Z)-Se-(3,5-dinitrobenzyl)-N-cyano-N,N'-di(4-bromophenyl)isoselenourea 

Relevant articles and documents

Scalable, easy synthesis, and efficient isolation of arylnitromethanes: a revival of the Victor Meyer reaction

A modified approach to synthesize and isolate arylnitromethanes is described. The method takes advantage of the significant difference in acidity between the arylnitromethane and the major impurity of the reaction, the nitrite ester. The arylnitromethanes resulting from this process are obtained in high yields and are analytically pure, i.e., they do not require distillation or further purification, which is a comfortable improvement of the ancestral Victor Meyer reaction.

Solvent Effects on Proton Transfer Reactions: Benzoate Ion Promoted Deprotonation Reactions of Arylnitromethanes in Methanol Solution

Second-order rate constants and equilibrium constants have been determined for the benzoate ion promoted deprotonation reactions of (m-nitrophenyl)nitromethane, (p-nitrophenyl)nitromethane, and (3,5-dinitrophenyl)nitromethane in methanol solution. The pK