147021-86-1

Basic information

• Product Name: 3,4-DIAMINO-2-NITROTOLUENE
• Synonyms: 3,4-DIAMINO-2-NITROTOLUENE
• CAS NO: 147021-86-1
• Molecular Formula: C₇H₉N₃O₂
• Molecular Weight: 167.17
• Product Categories: pharmacetical
• Mol File: 147021-86-1.mol

Chemical Properties

• Boiling Point: 361.2°Cat760mmHg
• Flash Point: 172.2°C
• Appearance: /
• Density: 1.369g/cm³
• Vapor Pressure: 2.11E-05mmHg at 25°C
• Refractive Index: 1.679
• CAS DataBase Reference: 3,4-DIAMINO-2-NITROTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIAMINO-2-NITROTOLUENE(147021-86-1)
• EPA Substance Registry System: 3,4-DIAMINO-2-NITROTOLUENE(147021-86-1)

Safety Data

• Hazardous Substances Data: 147021-86-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H9N3O2/c1-4-2-3-5(8)6(9)7(4)10(11)12/h2-3H,8-9H2,1H3

Upstream product

• 2160-10-3 5-methyl-4-nitrobenzo-2,1,3-selenadiazole 
• 496-72-0 4-methyl-1,2-diaminobenzene 
• 1123-91-7 5-Methyl-benzo[1,2,5]selenadiazole 
• 89-62-3 4-methyl-2-nitroaniline 
• 344749-24-2 6-chloro-3-methyl-2-nitro-aniline 

Downstream Products

• 90349-14-7 2,5-dimethyl-4-nitro-1H-benzimidazole 
• 31995-60-5 7(4)-nitro-6(5)-methyl-1H-benzo[1.2.3]triazole 
• 205502-10-9 2,3,6-trimethyl-5-aminoquinoxaline 
• 205502-09-6 5-hydroxy-2,3,6-trimethylquinoxaline 
• 3152-87-2 4-nitro-5-methylbenzo-2,1,3-thiadiazole 

Relevant articles and documents

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A novel series of highly potent benzimidazole-based microsomal triglyceride transfer protein inhibitors

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Photoinduced Nitro-Nitrite Rearrangement of 5-Nitroquinoxalines

Unlike known o-nitro methyl derivatives of aromatic compounds, 6-methyl-5-nitro-, 2,3,6-trimethyl-5-nitro-, and 7-methyl-6-nitroquinoxaline and 1,6-dimethyl-5-nitroquinoxalinium perchlorate do not exhibit photochromism in aqueous-ethanolic solutions under conditions of flash photolysis with a time resolution of 50 μs. Under conditions of continuous photolysis, these 5-nitromethylquinoxaline derivatives and also 5-nitroquinoxaline undergo nitro-nitrite rearrangement to give 5-quinoxalinol derivatives with quantum yields ranging from 1 × 10-4 to 3 × 10-3; the efficiency of the photochemical reaction increases when irradiation is performed with a shorter-wave light. 6-Nitro derivatives do not form stable products of photochemical transformations under the same conditions.

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