13122-36-6

Basic information

• Product Name: nitrobenzene-4-d
• Synonyms: nitrobenzene-4-d
• CAS NO: 13122-36-6
• Molecular Weight: 124.103
• Mol File: 13122-36-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: nitrobenzene-4-d(CAS DataBase Reference)
• NIST Chemistry Reference: nitrobenzene-4-d(13122-36-6)
• EPA Substance Registry System: nitrobenzene-4-d(13122-36-6)

Safety Data

• Hazardous Substances Data: 13122-36-6(Hazardous Substances Data)

Upstream product

• 56075-39-9 1-(methylsulfonyl)-2-(4-nitrophenyl)diazene 
• 56075-38-8 1-(methylsulfonyl)-2-(2-nitrophenyl)diazene 
• 586-78-7 para-nitrophenyl bromide 
• 2719-13-3 N'-(4-Nitro-phenyl)-N-acetyl-hydrazin 
• 100-16-3 4-nitrophenylhydrazone 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 2395-99-5 4-nitrophenyl radical 
• 10125-39-0 3,3-diethyl-1-(4-nitrophenyl)triaz-1-ene 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 7693-38-1 α-Chloro-4-nitrobenzyl phenyl sulfone 
• 35427-74-8 4,4'-dideuterioazobenzene 
• 35427-74-8 4,4'-dideuterioazobenzene 
• 114059-69-7 4,4'-dideuteroazoxybenzene 
• 95373-13-0 4,4'-dideuteriohydrazobenzene 

Relevant articles and documents

A mild dehydrazination reaction of arylhydrazines using nitric oxide in the presence of oxygen

A new dehydrazination reaction of arylhydrazines using nitric oxide and oxygen as a mild nitrosating agent is described. Taking advantage of non-aqueous and non-acidic medium appears to cause this novel selectivity as a counterpart of the azide synthesis by the conventional methods. The generally and reaction mechanism were also investigated.

A preparing method of deuterated aromatic compounds

The invention belongs to the field of chemical synthesis, particularly a preparing method of deuterated aromatic compounds. The method includes subjecting an aryl halide, as an initial raw material, to a palladium catalyzed carbon-halogen bond reduction r

Efficient Route to Deuterated Aromatics by the Deamination of Anilines

One-step replacement of NH2 groups in ring-substituted anilines by deuterium is reported. Approaches comprising both solid-phase and solution-phase syntheses can be used on a large variety of substrates. The method uses diazotization in a mixture of water and either dichloromethane or chloroform, which serve as a source of hydrogen. This protocol can be used as a general method for fast and easy incorporation of deuterium into an aromatic system using deuterated chloroform.