5473-06-3

Basic information

• Product Name: 1H-Benzimidazole,5-methyl-2-propyl-(9CI)
• Synonyms: 1H-Benzimidazole,5-methyl-2-propyl-(9CI)
• CAS NO: 5473-06-3
• Molecular Formula: C₁₁H₁₄N₂
• Molecular Weight: 174.24226
• Product Categories: BENZIMIDAZOLE
• Mol File: 5473-06-3.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 363.6°Cat760mmHg
• Flash Point: 185.7°C
• Appearance: /
• Density: 1.084g/cm³
• Vapor Pressure: 3.74E-05mmHg at 25°C
• Refractive Index: 1.608
• CAS DataBase Reference: 1H-Benzimidazole,5-methyl-2-propyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole,5-methyl-2-propyl-(9CI)(5473-06-3)
• EPA Substance Registry System: 1H-Benzimidazole,5-methyl-2-propyl-(9CI)(5473-06-3)

Safety Data

• Hazardous Substances Data: 5473-06-3(Hazardous Substances Data)

Usage

Heterocyclic compound

1H-Benzimidazole,5-methyl-2-propyl-(9CI) is a compound that contains a benzene ring fused to an imidazole ring.

Chemical applications

1H-Benzimidazole,5-methyl-2-propyl-(9CI) is used in various chemical applications due to its unique structure and reactivity.

Pharmaceutical applications

It has potential applications in drug development.

Chemical intermediate

It can be used as a chemical intermediate in organic synthesis.

Research and development

Its properties and uses make it an interesting target for further research and development in the field of chemistry and pharmaceuticals.

InChI:InChI=1/C11H14N2/c1-3-4-11-12-9-6-5-8(2)7-10(9)13-11/h5-7H,3-4H2,1-2H3,(H,12,13)

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Relevant articles and documents

Activated alumina ball catalyzed expeditious synthesis of 2-alkylbenzimidazoles with special emphasis on susceptible side chains possessing amide functionality

A solvent- and chromatography-free, non-hazardous green protocol for the synthesis of 2-alkylbenzimidazoles has been developed under neutral conditions with water as the only by-product. Activated alumina balls, which have been shown previously to assist in amidation reaction, also catalyze very successfully the condensation of benzene-1,2-diamines with carboxylic acids to produce the corresponding benzimidazoles. This methodology is also applicable to susceptible side chains possessing an amide functionality.

Synthesis of α-chloroaldoxime O-methanesulfonates and their use in the synthesis of functionalized benzimidazoles

Three different α-chloroaldoxime O-methanesulfonates were synthesized to investigate their chemical properties. The compounds were found to be stable and were able to be stored at ambient temperature without any precautions. The reactions with anilines we

Copper-catalyzed synthesis of benzimidazoles via cascade reactions of o-haloacetanilide derivatives with amidine hydrochlorides

(Chemical Equation Presented) We have developed an efficient method for the synthesis of benzimidazoles via cascade reactions of o-haloacetoanilide derivatives with amidine hydrochlorides. The protocol uses 10 mol % CuBr as the catalyst, CS2CO