53953-47-2

Basic information

• Product Name: 1H-Benzimidazole-1-propanol(9CI)
• Synonyms: 1H-Benzimidazole-1-propanol(9CI);3-(1-benzimidazolyl)propan-1-ol;3-(1H-benzimidazol-1-yl)propan-1-ol;3-(benzimidazol-1-yl)propan-1-ol
• CAS NO: 53953-47-2
• Molecular Formula: C10H12N2O
• Molecular Weight: 176.22
• Product Categories: BENZIMIDAZOLE
• Mol File: 53953-47-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Benzimidazole-1-propanol(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole-1-propanol(9CI)(53953-47-2)
• EPA Substance Registry System: 1H-Benzimidazole-1-propanol(9CI)(53953-47-2)

Safety Data

• Hazardous Substances Data: 53953-47-2(Hazardous Substances Data)

Usage

Chemical class

Benzimidazole derivative

Structural feature

Contains a propanol group

Potential applications

Medicinal chemistry

Pharmaceutical development

Development of pharmaceutical drugs

Biological activities

Antiparasitic, antiviral, and anticancer properties

Propanol group effect

May enhance existing activities or impart new beneficial properties

Further research

Necessary to determine specific pharmacological and therapeutic potential

Testing

Required to confirm the compound's potential in the medical field
These properties and contents provide a brief overview of 1H-Benzimidazole-1-propanol (9CI) and its potential significance in the field of medicinal chemistry and pharmaceutical drug development.

Upstream product

• 51-17-2 benzoimidazole 
• 627-18-9 1-bromo-3-propanol 
• 2453-03-4 trimethylene carbonate 
• 627-30-5 1-chloro-3-hydroxypropane 

Downstream Products

• 151029-72-0 1-(Benzimidazol-1-yl)-3-chloropropane 

Relevant articles and documents

Synthesis of N-heterocyclic nitrenium (NHN) ions and related donor systems: Coordination with d10-metal ions

The synthesis of three new NNN- and CNC type N-heterocyclic nitrenium (NHN) ion based pincer ligands is reported from 1,3-di-(2′-bromoethyl)-triazolium bromide (5). The reaction of 5 with ammonium hexafluorophosphate followed by two equivalent of pyrrolid

N-Alkylation of Imidazoles with Dialkyl and Alkylene Carbonates

Abstract: The reactions of imidazoles with a series of dialkyl and alkylene carbonatesafforded the corresponding N-alkyl- andN-(hydroxyalkyl)imidazoles with highyields. The reactivity of dialkyl carbonates decreases in the series dimethyl> diethyl > dibutyl carbonate. Ethylene carbonate is a more efficientalkylating agent than trimethylene carbonate. The mechanisms of alkylation ofimidazole with dimethyl carbonate and ethylene carbonate were studied by DFTquantum chemical calculations at the B3LYP/6-311++G(d,p) level of theory.

Agent for use as an anti-irritant

The use of a compound having the formula STR1 or a cosmetically acceptable acid addition salt form thereof, for preventing or reducing irritation or itching of the skin of human beings; cosmetic compositions comprising said agents, processes for preparing