608-32-2

Basic information

• Product Name: 1,2,3-TRIAMINOBENZENE
• Synonyms: 1,2,3-benzenetriamine
• CAS NO: 608-32-2
• Molecular Formula: C₆H₉N₃
• Molecular Weight: 123.16
• Mol File: 608-32-2.mol
• Article Data: 14

Chemical Properties

• Melting Point: 103°C
• Boiling Point: 219.27°C (rough estimate)
• Flash Point: 179.2°C
• Appearance: /
• Density: 1.1097 (rough estimate)
• Vapor Pressure: 0.000115mmHg at 25°C
• Refractive Index: 1.5589 (estimate)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 4.50±0.50(Predicted)
• CAS DataBase Reference: 1,2,3-TRIAMINOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-TRIAMINOBENZENE(608-32-2)
• EPA Substance Registry System: 1,2,3-TRIAMINOBENZENE(608-32-2)

Safety Data

• Hazardous Substances Data: 608-32-2(Hazardous Substances Data)

Usage

General Description

1,2,3-Triaminobenzene, often represented as C6H6N3, is a chemical compound that belongs to the family of benzenes and derivatives. It is also known by names which include m-phenylenediamine. This organic compound is characterized by three amine groups (NH2) attached to a benzene ring. It finds extensive use in organic synthesis environments, and is a starting material for more complex compounds in the field of chemistry. There is limited safety or toxicity information available on this compound, thus care must be employed in its handling and usage.

InChI:InChI=1/C6H9N3/c7-4-2-1-3-5(8)6(4)9/h1-3H,7-9H2

Upstream product

• 602-03-9 2,3-dinitroaniline 
• 606-22-4 2,6-dinitroaniline 
• 618-77-9 3,4,5-triamino-benzoic acid 
• 7647-01-0 hydrogenchloride 
• 16322-19-3 4-nitro-2,1,3-benzoxadiazole 
• 88-88-0 2,4,6-trinitrochlorobenzene 
• 606-21-3 1-chloro-2,6-dinitrobenzene 
• 95-54-5 1,2-diamino-benzene 
• 20718-41-6 4-nitro-2,1,3-benzoselenadiazole 
• 273-15-4 piazselenole 
• 3694-52-8 2,3-diamino-nitrobenzene 
• 30417-18-6 N-benzyl-2,6-dinitroaniline 

Downstream Products

• 16566-20-4 quinoxalin-5-ylamine 
• 767-65-7 4-amino-2,1,3-benzoselenadiazole 
• 30905-08-9 N-(2-methyl-1(3)H-benzimidazol-4-yl)-acetamide 
• 96013-05-7 2-methyl-4-aminobenzimidazole 
• 137654-47-8 4(7)-formylbenzimidazole 
• 75370-65-9 4-amino-1,3-dihydro-benzimidazole-2-one 
• 928388-13-0 C₁₄H₁₉N₃O 

Relevant articles and documents

(AZA)INDOLE-, BENZOTHIOPHENE-, AND BENZOFURAN-3-SULFONAMIDES

Disclosed are sulfonamide compounds with GPR17 modulating properties, which are useful for treating or preventing a variety of CNS and other diseases, in particular for preventing and treating myelinating diseases or disorders.

Trinuclear {Co2+-M3+-Co2+} complexes catalyze reduction of nitro compounds

This work presents synthesis and characterization of trinuclear {Co2+-Co3+-Co2+} and {Co2+-Fe3+-Co2+} complexes with accessible peripheral Co(ii) ions. Both trinuclear complexes function as efficient reusable heterogeneous catalysts for the selective reduction of assorted nitro compounds to the corresponding amines. The mechanistic investigations suggest the involvement of a Co(ii)-Co(i) cycle in the catalysis.

Fast and efficient reduction of nitro aromatic compounds over Fe 3O4/β-alanine-acrylamide-Ni nanocomposite as a new magnetic catalyst

In this study, Ni nanoparticles incorporated β-alanine-acrylamide (Ala-AA) was successfully prepared by a simple method. The obtained magnetic nanocomposite exhibited excellent activity as a new heterogeneous magnetic catalyst for the reduction of a numbe