29043-48-9

Basic information

• Product Name: 1H-Benzimidazol-5-amine,2-methyl-(9CI)
• Synonyms: 1H-Benzimidazol-5-amine,2-methyl-(9CI);5-AMINO-2-METHYLBENZIMIDAZOLE;2-Methyl-3H-benzoimidazol-5-ylamine monohydrochloride;2-methyl-1H-benzimidazol-5-amine;(2-methyl-3H-benzimidazol-5-yl)amine;2-methyl-3H-benzimidazol-5-amine;2-methyl-1H-benzimidazol-6-amine(SALTDATA: 2HCl);2-Methyl-5-aMinobenziMidazole
• CAS NO: 29043-48-9
• Molecular Formula: C₈H₉N₃
• Molecular Weight: 147.18
• Product Categories: BENZIMIDAZOLE
• Mol File: 29043-48-9.mol
• Article Data: 1

Chemical Properties

• Melting Point: 95℃
• Boiling Point: 441.1 °C at 760 mmHg
• Flash Point: 250.8 °C
• Appearance: /
• Density: 1.295
• Vapor Pressure: 1.89E-08mmHg at 25°C
• Storage Temp.: 2-8°C(protect from light)
• PKA: 12.57±0.10(Predicted)
• CAS DataBase Reference: 1H-Benzimidazol-5-amine,2-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazol-5-amine,2-methyl-(9CI)(29043-48-9)
• EPA Substance Registry System: 1H-Benzimidazol-5-amine,2-methyl-(9CI)(29043-48-9)

Safety Data

• Hazardous Substances Data: 29043-48-9(Hazardous Substances Data)

Usage

General Description

1H-Benzimidazol-5-amine,2-methyl-(9CI) is a chemical compound with the molecular formula C8H9N3. It is a derivative of benzimidazole, which is a fused heterocyclic compound containing a benzene ring fused to an imidazole ring. This chemical has one methyl group attached to the benzimidazole ring. It is used in the pharmaceutical industry for the synthesis of various pharmaceutical drugs. It has potential applications in the field of medicinal chemistry and drug discovery due to its unique structure and properties. The compound is also used as a building block in organic synthesis to create new molecules with specific biological activities.

InChI:InChI=1/C8H9N3.ClH/c1-5-10-7-3-2-6(9)4-8(7)11-5;/h2-4H,9H2,1H3,(H,10,11);1H

Upstream product

• 64170-55-4 4-(5-methyl-tetrazol-1-yl)-aniline 

Downstream Products

• 56842-62-7 5-acetamido-2-methylbenzimidazole 
• 76152-82-4 (2,4-dinitro-phenyl)-(2-methyl-1⁽³⁾H-benzimidazol-5-yl)-amine 
• 56842-63-8 C₁₅H₁₄N₄O 
• 1403816-03-4 N-(2-methyl-1H-benzo[d]imidazol-5-yl)-5-phenyl-1H-pyrazolo[4,3-d]pyrimidin-7-amine 
• 1403818-70-1 N-(2-methyl-1H-benzo[d]imidazol-5-yl)-5-(3-(methylsulfonyl)phenyl)-1H-pyrazolo[4,3-d]pyrimidin-7-amine 
• 1089671-53-3 C₂₁H₁₇FN₄O 
• 686747-52-4 3-chloro-N-[1-(3-chloro-2-methylbenzenesulphonyl)-2-methyl-1H-benzoimidazol-5-yl]-2-methylbenzenesulphonamide 
• 686747-53-5 3-chloro-N-[1-(3-chloro-2-methylbenzenesulphonyl)-2-methyl-1H-benzoimidazol-6-yl]-2-methylbenzenesulphonamide 
• 73857-51-9 2,7,8-trimethyl-3,6-dihydro-imidazo[4,5-e]indole 
• 73857-40-6 2,8-Dimethyl-7-phenyl-3,6-dihydro-imidazo[4,5-e]indole 

Relevant articles and documents

THERMAL REACTIONS OF 1-ARYL-5-METHYLTETRAZOLES

The mechanism of the thermal reactions of 1-aryl-5-methyltetrazoles, which involve isomerization to the azide, elimination of a nitrogen molecule, and formation of singlet nitrenes followed by isomerization to benzimidazoles and carbodiimides, has been studied by combinig the methods of derivatography and the current arsenal of mass-spectrometric techniques.The influence of the electronic properties of the substituent (in the para position of the benzene ring) on the course of the thermolysis has been established.