39235-92-2

Basic information

• Product Name: N*1*-BENZYL-4-CHLORO-BENZENE-1,2-DIAMINE
• Synonyms: N-BENZYL-4-CHLORO-BENZENE-1,2-DIAMINE
• CAS NO: 39235-92-2
• Molecular Formula: C₁₃H₁₃ClN₂
• Molecular Weight: 232.70872
• Mol File: 39235-92-2.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 407.3 °C at 760 mmHg
• Flash Point: 200.1 °C
• Appearance: /
• Density: 1.265 g/cm³
• Vapor Pressure: 7.65E-07mmHg at 25°C
• Refractive Index: 1.68
• CAS DataBase Reference: N*1*-BENZYL-4-CHLORO-BENZENE-1,2-DIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N*1*-BENZYL-4-CHLORO-BENZENE-1,2-DIAMINE(39235-92-2)
• EPA Substance Registry System: N*1*-BENZYL-4-CHLORO-BENZENE-1,2-DIAMINE(39235-92-2)

Safety Data

• Hazardous Substances Data: 39235-92-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H13ClN2/c14-11-6-7-13(12(15)8-11)16-9-10-4-2-1-3-5-10/h1-8,16H,9,15H2

Upstream product

• 2948-37-0 N-(4-chlorophenyl)benzylamine 
• 345-18-6 2-fluoro-5-chloronitrobenzene 
• 100-46-9 benzylamine 
• 100-39-0 benzyl bromide 
• 95-83-0 4-Chloro-1,2-phenylenediamine 
• 100-44-7 benzyl chloride 
• 89-63-4 4-Chloro-2-nitroaniline 
• 10066-18-9 N-benzyl-4-chloro-2-nitrobenzenamine 

Downstream Products

• 39235-96-6 1-benzyl-5-chloro-2-phenyl-1H-benzo[d]imidazole 
• 1382488-21-2 1-benzyl-5-chloro-2-[1-(4-isobutylphenyl)ethyl]-1H-benzimidazole 
• 1382488-19-8 N-(2-(benzylamino)-5-chlorophenyl)-2-(4-isobutylphenyl)propanamide 
• 53703-82-5 1-benzyl-5-chloro-2-(4-methylphenyl)-1H-benzimidazole 
• 1415650-63-3 1-benzyl-2-(4-(benzyloxy)phenyl)-5-chloro-1H-benzimidazole 
• 4926-65-2 6‐chloro‐2‐phenyl‐1H-benzoimidazole 
• 53703-98-3 4-(1-benzyl-6-chloro-1H-benzo[d]imidazol-2-yl)phenol 
• 53703-87-0 2-(benzo[d] [1,3] dioxol-5-yl)-1-benzyl-5-chloro-1H-benzo[d]imidazole 

Relevant articles and documents

Novel benzimidazole-triazole hybrids as apoptosis inducing agents in lung cancer: Design, synthesis, 18F-radiolabeling & galectin-1 inhibition studies

In this study, we have synthesized a new series of benzimidazole-triazole hybrids as galectin-1 (gal-1) mediated apoptosis-inducing agents, and evaluated for their potential anticancer activity against a panel of human cancer cell lines viz. breast cancer

Regioselective Nitration of N-Alkyl Anilines using tert-Butyl Nitrite under Mild Condition

Regioselective ring nitration of N-alkyl anilines is reported using tert-butyl nitrite. The reactions proceed efficiently with a wide range of substrates providing synthetically useful N-nitroso N-alkyl nitroanilines in excellent yields which can be easily converted into N-alkyl phenylenediamines and N-alkyl nitroanilines using Zn-AcOH and HCl/MeOH, respectively.

Synthesis of substituted phenanthrene-9-benzimidazole conjugates: Cytotoxicity evaluation and apoptosis inducing studies

A series of new phenanthrene-9-benzimidazole conjugates has been synthesized by condensing phenanthrene aldehydes with various substituted o-phenylenediamines. The title compounds were evaluated for their in vitro cytotoxic potential against various human