6971-33-1

Basic information

• Product Name: 3-NITRO-4-NITROSOTOLUENE
• Synonyms: 3-NITRO-4-NITROSOTOLUENE;4-Methyl-2-nitro-1-nitrosobenzene
• CAS NO: 6971-33-1
• Molecular Formula: C₇H₆N₂O₃
• Molecular Weight: 166.13414
• Mol File: 6971-33-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 319.3°Cat760mmHg
• Flash Point: 146.9°C
• Appearance: /
• Density: 1.34g/cm³
• Vapor Pressure: 0.000639mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: 3-NITRO-4-NITROSOTOLUENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITRO-4-NITROSOTOLUENE(6971-33-1)
• EPA Substance Registry System: 3-NITRO-4-NITROSOTOLUENE(6971-33-1)

Safety Data

• Hazardous Substances Data: 6971-33-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H6N2O3/c1-5-2-3-6(8-10)7(4-5)9(11)12/h2-4H,1H3

Upstream product

• 610-39-9 3,4-Dinitrotoluene 
• 89-62-3 4-methyl-2-nitroaniline 
• 7732-18-5 water 
• 67-56-1 methanol 
• 7803-49-8 hydroxylamine 

Downstream Products

• 118725-15-8 (2-chloro-phenyl)-(4-methyl-2-nitro-phenyl)-diazene 
• 474318-51-9 5-methyl-2-nitronitrosobenzene 
• 105946-25-6 2-(2-chloro-phenyl)-6-methyl-2H-benzotriazole-1-oxide 
• 113550-94-0 2-(2-chloro-phenyl)-5-methyl-2H-benzotriazole 
• 114462-03-2 5-methyl-2-(2',4'-dimethoxyphenyl)-2H-benzotriazole 
• 114461-99-3 2-(2-Methoxy-phenyl)-5-methyl-2H-benzotriazole 
• 38610-48-9 2-(4'-methoxyphenyl)-5-methyl-2H-benzotriazole 
• 114462-05-4 4-(5'-methyl-2'H-benzotriazol-2'-yl)phenol 
• 134859-18-0 11-benzoyldibenzophenazine 
• 216387-91-6 phenyl(2,3-diphenyl-6-quinoxalinyl)carbinol 
• 150252-47-4 6-benzoyl-2,3-diphenylquinoxaline 
• 119426-73-2 (2,3-dimethylquinoxalin-6-yl)(phenyl)methanone 
• 57070-71-0 (3,4-diaminophenyl)phenylmethanone hydrochloride 
• 39070-63-8 4-benzoylbenzene-1,2-diamine 

Relevant articles and documents

6-Lithioquinoxalines and Their Transformations

6-Bromo-2,3-diphenylquinoxaline reacts with butyllithium to give the 6-lithio derivative in a yield of more than 80%, which reacts with electrophiles such as benzophenone, Michler ketone, methyl ethyl ketone, iodine, selenium, and dimethylformamide to give the corresponding quinoxaline derivatives. 6-Bromo-2,3-dimethylquinoxaline is metallated with butyl- and phenyllithium at the methyl groups and benzene ring. These organolithium compounds react with benzophenone to give the corresponding diphenyl- and triaryl-carbinols, whose yield and ratio were determined by HPLC. These results open prospects for preparing new quinoxaline derivatives substituted at the annelated benzene ring.