57070-71-0

Basic information

• Product Name: 3,4-DIAMINOBENZOPHENONE MONOHYDROCHLORIDE
• Synonyms: 3,4-DIAMINOBENZOPHENONE MONOHYDROCHLORIDE;3,4-diaminobenzophenone hydrochloride;3,4-DiaminobenzophenoneHCl;3,4-DIAMINOBENZOPHENONE MONOHYDROCHLORIDE 97%;3,4-Diaminobenzophenone monohydrochloride,97%;VNCHICMXBKDTOS-UHFFFAOYSA-N
• CAS NO: 57070-71-0
• Molecular Formula: C₁₃H₁₂N₂O*ClH
• Molecular Weight: 248.71
• EINECS: 260-541-5
• Mol File: 57070-71-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 210-215 °C
• Boiling Point: 440.7 °C at 760 mmHg
• Flash Point: 220.3 °C
• Appearance: GREENISH TO DARK BROWN GRANULAR CRYSTALLINE POWDER
• Density: 1.233g/cm³
• Vapor Pressure: 5.76E-08mmHg at 25°C
• CAS DataBase Reference: 3,4-DIAMINOBENZOPHENONE MONOHYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DIAMINOBENZOPHENONE MONOHYDROCHLORIDE(57070-71-0)
• EPA Substance Registry System: 3,4-DIAMINOBENZOPHENONE MONOHYDROCHLORIDE(57070-71-0)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 57070-71-0(Hazardous Substances Data)

Usage

Chemical Properties

GREENISH TO DARK BROWN GRANULAR CRYSTALLINE POWDER

InChI:InChI=1/C13H12N2O.ClH/c14-11-7-6-10(8-12(11)15)13(16)9-4-2-1-3-5-9;/h1-8H,14-15H2;1H

Upstream product

• 89-62-3 4-methyl-2-nitroaniline 
• 33609-48-2 3,4-dinitrobenzophenone 
• 6971-33-1 4-methyl-2-nitro-1-nitrosobenzene 
• 610-39-9 3,4-Dinitrotoluene 
• 528-45-0 3,4-dinitrobenzoic acid 

Downstream Products

• 104273-37-2 Potassium salt of 5-benzoyl-2-thiobenzimidazole 
• 104273-56-5 6-<5-Benzoylbenzimidazol-2-yl-thio>hexanoic Acid 
• 104273-41-8 Diethyl-thiocarbamic acid S-(5-benzoyl-1H-benzoimidazol-2-yl) ester 
• 104273-42-9 Dimethyl-dithiocarbamic acid 5-benzoyl-1H-benzoimidazol-2-yl ester 
• 104273-49-6 (5-phenylcarbonyl-1H-benzimidazol-2-ylthio)acetic acid 
• 108227-95-8 2-acetamido-5⁽⁶⁾-benzoylbenzimidazole 
• 52329-60-9 (2-amino-1H-benzo[d]imidazol-6-yl)(phenyl)methanone 
• 86260-70-0 {2-[4-(3-Ethylaminomethyl-4-methoxy-phenylamino)-6-trifluoromethyl-pyrimidin-2-ylamino]-1H-benzoimidazol-5-yl}-phenyl-methanone; hydrochloride 
• 86260-71-1 (2-{4-[4-Hydroxy-3-(4-methyl-piperazin-1-ylmethyl)-phenylamino]-6-trifluoromethyl-pyrimidin-2-ylamino}-1H-benzoimidazol-5-yl)-phenyl-methanone 
• 86260-69-7 {2-[4-(3-Diethylaminomethyl-4-methoxy-phenylamino)-6-trifluoromethyl-pyrimidin-2-ylamino]-1H-benzoimidazol-5-yl}-phenyl-methanone 
• 86260-68-6 {2-[4-(3-Diethylaminomethyl-4-hydroxy-phenylamino)-6-trifluoromethyl-pyrimidin-2-ylamino]-1H-benzoimidazol-5-yl}-phenyl-methanone 
• 86272-02-8 <<2-<<4-chloro-6-(trifluormethyl)-2-pyrimidinyl>amino>-1H-benzimidazol-5-yl>phenyl>methanone 
• 31431-39-7 mebendazole 
• 104662-93-3 5-Benzoyl-2-methoxycarbonylamino-benzoimidazole-1-carboxylic acid methyl ester 

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.