261764-92-5

Basic information

• Product Name: 1,3-BENZENEDIAMINE, 2-CHLORO-4-NITRO-
• Synonyms: 1,3-BENZENEDIAMINE, 2-CHLORO-4-NITRO-;4-CHLORO-6-NITRO-M-PHENYLENE DIAMINE;2-Chloro-4-nitro-1,3-phenylenediamine;4-Chloro-6-nitrobenzene-1,3-diaMine;2-Chloro-4-nitrobenzene-1,3-diaMine;2-Chloro-4-nitro-m-phenylenediamine
• CAS NO: 261764-92-5
• Molecular Formula: C₆H₆ClN₃O₂
• Molecular Weight: 187.58
• Mol File: 261764-92-5.mol

Chemical Properties

• Boiling Point: 393.2 °C at 760 mmHg
• Flash Point: 191.6 °C
• Appearance: /
• Density: 1.592 g/cm³
• Storage Temp.: 2-8°C(protect from light)
• PKA: -1.06±0.14(Predicted)
• CAS DataBase Reference: 1,3-BENZENEDIAMINE, 2-CHLORO-4-NITRO-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-BENZENEDIAMINE, 2-CHLORO-4-NITRO-(261764-92-5)
• EPA Substance Registry System: 1,3-BENZENEDIAMINE, 2-CHLORO-4-NITRO-(261764-92-5)

Safety Data

• Hazardous Substances Data: 261764-92-5(Hazardous Substances Data)

Usage

Uses

Used in Polymer Industry:
1,3-Benzenediamine, 2-chloro-4-nitrois used as a monomer in the industrial manufacture of polyamide. It contributes to the formation of polymer separation films, which are essential in the process of separating volatile organic compounds (VOCs) from the air or other gas mixtures. The presence of the chlorine and nitro groups in the compound enhances its reactivity and compatibility with other monomers, resulting in the production of high-quality polyamide films with improved separation capabilities.

Upstream product

• 261764-91-4 2,3-dichloro-4-nitroacetanilide 
• 23068-36-2 N-(2,3-dichlorophenyl)-acetamide 

Downstream Products

• 269-08-9 1H-imidazo[4,5-g]quinoline 
• 261764-96-9 6,7-diaminoquinoline 

Relevant articles and documents

Synthesis of two novel tricyclic rings: Triazolo[4,5-g]- quinolines and pyrido[2,3-g]quinoxalines derived from 6,7-diaminoquinolines

A general simple route for the synthesis of triazolo[4,5-g]quinolines and pyrido[2,3-g]quinoxalines is described. The heterocycles obtained were fully characterised by their spectroscopical properties. A revision of the nitration of the 2,3-dichloroacetanilide is also discussed, since it afforded the request nitro derivative to build up the key intermediate 6,7- diaminoquinolines.