7187-47-5

Basic information

• Product Name: 4-(1H-BENZIMIDAZOL-2-YL)-1,3-THIAZOL-2-AMINE
• Synonyms: 4-(1H-BENZIMIDAZOL-2-YL)-1,3-THIAZOL-2-AMINE;Albb-007425;4-(1H-benzimidazol-2-yl)-1,3-thiazol-2-amine(SALTDATA: FREE);[4-(1H-benzimidazol-2-yl)thiazol-2-yl]amine;4-(1H-benzimidazol-2-yl)-2-thiazolamine;4-(1H-benzimidazol-2-yl)thiazol-2-amine;4-(1H-Benzoimidazol-2-yl)-thiazol-2-ylamine
• CAS NO: 7187-47-5
• Molecular Formula: C10H8N4S
• Molecular Weight: 216.27
• Mol File: 7187-47-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 516.8°C at 760 mmHg
• Flash Point: 266.4°C
• Appearance: /
• Density: 1.487g/cm³
• Vapor Pressure: 8.69E-11mmHg at 25°C
• Refractive Index: 1.796
• CAS DataBase Reference: 4-(1H-BENZIMIDAZOL-2-YL)-1,3-THIAZOL-2-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1H-BENZIMIDAZOL-2-YL)-1,3-THIAZOL-2-AMINE(7187-47-5)
• EPA Substance Registry System: 4-(1H-BENZIMIDAZOL-2-YL)-1,3-THIAZOL-2-AMINE(7187-47-5)

Safety Data

• Hazardous Substances Data: 7187-47-5(Hazardous Substances Data)

Usage

General Description

4-(1H-benzimidazol-2-yl)-1,3-thiazol-2-amine is a chemical compound with the molecular formula C9H7N5S. It is an organic compound that belongs to the families of benzimidazoles and thiazoles. It is a heterocyclic compound that contains both nitrogen and sulfur in its structure. This chemical may have potential applications in pharmaceuticals, agriculture, and material science. It is important to handle this chemical with care and follow proper safety precautions when working with it in a laboratory or industrial setting. Further research and experimentation may be necessary to fully understand the properties and potential uses of 4-(1H-benzimidazol-2-yl)-1,3-thiazol-2-amine.

InChI:InChI=1/C10H8N4S/c11-10-14-8(5-15-10)9-12-6-3-1-2-4-7(6)13-9/h1-5H,(H2,11,14)(H,12,13)

Upstream product

• 17356-08-0 thiourea 
• 939-70-8 2-acetylbenzimidazole 
• 10227-63-1 1-(1H-benzo[d]imidazol-2-yl)-2-bromoethanone 

Downstream Products

• 1427160-26-6 [4-(1H-benzoimidazol-2-yl)thiazol-2-yl](benzylidene)amine 
• 1427160-27-7 [4-(1H-benzoimidazol-2-yl)thiazol-2-yl](4-nitrobenzylidene)amine 
• 1427160-28-8 [4-(1H-benzoimidazol-2-yl)thiazol-2-yl](4-bromobenzylidene)amine 
• 1427160-29-9 N-(4-methoxybenzylidene)-4-(1H-benzo[d]imidazol-2-yl)thiazol-2-amine 
• 1443114-18-8 2-(2-(2-(2,6-difluorobenzamido)thiazol-4-yl)-1H-benzo[d]imidazol-1-yl)acetic acid 
• 1443114-16-6 2,6-difluoro-N-(4-(1-isopropyl-1H-benzo[d]imidazol-2-yl)thiazol-2-yl)benzamide 
• 1443114-17-7 ethyl 2-(2-(2-(2,6-difluorobenzamido)thiazol-4-yl)-1H-benzo[d]imidazol-1-yl)acetate 
• 1443114-15-5 N-(4-(1H-benzo[d]imidazol-2-yl)thiazol-2-yl)-2,6-difluorobenzamide 

Relevant articles and documents

Synthesis of Some Benzimidazole-based Heterocycles and their Application as Copper Corrosion Inhibitors

A series of new substituted benzimidazoles embedded with a variety of function groups has been synthesized from N-methyl-2-bromoacetylbenzimidazole. The synthesized compounds were fully characterized, and their structures were elucidated based on elemental analysis, spectral data, and alternative synthetic pathways, whenever possible. Some of benzimidazole derivatives were tested as corrosion inhibitors.

Synthesis and biological evaluation of some novel [4-(1H-Benzoimidazol-2- yl)-thiazol-2-yl]-benzylidene-amines and N-[4-(1H-Benzoimidazol-2-yl)-thiazol-2- yl]-N'-benzylidene-hydrazines

A new family of thiazole heterocycles, namely [4-(1H-benzoimidazol-2-yl)- thiazol-2-yl]-benzylidene-amines has been synthesized by the condensation of 4-(1H-Benzoimidazol-2-yl)-thiazol-2-ylamine with various aromatic aldehydes and N-[4-(1H-benzoimidazol-2-yl)-thiazol-2-yl]-N'-benzylidene-hydrazines through the cyclization of 1-(1H-benzoimidazol-2-yl)-2-bromo-ethanone with arylthiosemicarbazones. The target compounds are achieved by using 1-(1H-Benzoimidazol-2-yl)-ethanone as starting material. The chemical structures of all newly synthesized compounds were confirmed by their IR, 1H NMR and Mass spectral data. Further the compounds were used to evaluate their antimicrobial activity and found that the appreciable antimicrobial activity by some of the title compounds.