53464-31-6

Basic information

• Product Name: 1-(4-nitrophenyl)-3,3'-methylphenyltriazene
• Synonyms: 1-(4-nitrophenyl)-3,3'-methylphenyltriazene
• CAS NO: 53464-31-6
• Molecular Weight: 256.264
• Mol File: 53464-31-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-(4-nitrophenyl)-3,3'-methylphenyltriazene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-nitrophenyl)-3,3'-methylphenyltriazene(53464-31-6)
• EPA Substance Registry System: 1-(4-nitrophenyl)-3,3'-methylphenyltriazene(53464-31-6)

Safety Data

• Hazardous Substances Data: 53464-31-6(Hazardous Substances Data)

Upstream product

• 14368-49-1 p-nitrobenzenediazonium 
• 100-61-8 N-methylaniline 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 64-17-5 ethanol 
• 40078-29-3 4-nitro-benzenediazo hydroxide 
• 21857-39-6 p-nitrobenzenediazo methyl ether 
• 100-05-0 4-nitrobenzenediazonium chloride 
• 127-09-3 sodium acetate 
• 74-89-5 methylamine 
• 100-01-6 4-nitro-aniline 
• 121-69-7 N,N-dimethyl-aniline 

Downstream Products

• 607-27-2 2-(2-(4-nitrophenyl)diazenyl)naphth-1-ol 
• 5290-62-0 1-hydroxy-4-(4-nitrophenylazo)naphthalene 
• 31464-31-0 N-methyl-4-nitro-4'-aminoazobenzene 
• 6410-10-2 para red 
• 100-61-8 N-methylaniline 

Relevant articles and documents

Mechanism of Diazo Coupling Reactions. Part XXXII. The Diazoamino Rearrangement in 20percent Acetonitrile/Aqueous Buffers

The rearrangements of 4'-methoxy-N-methyl- and N-methyl-4'-nitro-diazoaminobenzene have been studied in 20percent acetonitrile/aqueous buffers.The reactions are specifically acid catalyzed and involve pre-equilibrium formation of amine and diazonium salt

MECHANISM OF AZO COUPLING. III. ROLE OF CROWN ETHER IN AZO COUPLING

The equilibrium constants for complexation of a diazonium cation with a crown ether, as determined from kinetic data on azo coupling with aromatic amines, increase with decreasing polarity of the solvent, indicating a predominant contribution of electrost

KINETICS OF ACID CATALYZED DECOMPOSITION OF SUBSTITUTED 1,3-DIPHENYL-3-METHYLTRIAZENES

Kinetics of the acid catalyzed decomposition of fifteen 1-substituted-1,3-diphenyl-3-methyltriazenes have been studied in 40percent aqueous ethanolic buffers at 25 deg C.The slope found for the dependence logkobs vs pH of the buffer is not equa