676464-97-4

Basic information

• Product Name: 2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride
• CAS NO: 676464-97-4
• Molecular Formula: C₉H₁₁Cl₂N₃
• Molecular Weight: 232.10974
• Mol File: 676464-97-4.mol

Chemical Properties

• CAS DataBase Reference: 2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride(676464-97-4)
• EPA Substance Registry System: 2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride(676464-97-4)

Safety Data

• Hazardous Substances Data: 676464-97-4(Hazardous Substances Data)

Usage

Uses

Given the provided materials, there are no specific applications listed for 2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride. However, based on its structure and the general properties of imidazo[4,5-c]pyridine derivatives, potential uses in various industries could include:
Used in Pharmaceutical Industry:
2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride could be used as a pharmaceutical intermediate for the development of new drugs, given its potential to interact with biological systems. Its specific structural features may allow it to target certain receptors or enzymes, making it a candidate for drug discovery and medicinal chemistry research.
Used in Chemical Research:
In the field of chemical research, 2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride may serve as a starting material for the synthesis of more complex molecules or for studying the reactivity of chloromethyl and ethyl groups in various chemical reactions.
Used in Material Science:
2-(chloromethyl)-3-ethyl-imidazo[4,5-c]pyridine hydrochloride might also find applications in material science, potentially being incorporated into the development of new materials with specific properties, such as sensors or catalysts, due to its reactivity and structural characteristics.

Upstream product

• 676464-98-5 (3-ethylaminopyridin-4-yl)carbamic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 54-96-6 3,4-diaminopyridine 
• 541-88-8 Chloroacetic anhydride 
• 676464-96-3 N-(4-aminopyridin-3-yl)acetamide hydrochloride 
• 61719-62-8 N-3-ethyl-pyridine-3,4-diamine 
• 688001-00-5 2-chloromethyl-3-ethyl-3H-imidazo[4,5-c]pyridine 
• 183311-28-6 (3-Amino-pyridin-4-yl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Regioselective synthesis of an imidazo[4,5-c]pyridine through selective acylation of 3,4-diaminopyridine: Synthesis of CP-885,316

CP-885,316 (1), an imidazo[4,5-c]pyridine, 4, was prepared from 3,4-diaminopyridine (9). Two routes were demonstrated using the regioselective introduction of either an acetamide at the 3-position or a tert-butylcarbamate at the 4-position.

Process for preparing haloalkyl pyrimidines

The invention is a process for producing haloalkyl pyrimidines as intermediates in the production of benzimidazole and/or pyridylimidazole derivatives having high selectivity and/or high affinity to the benzodiazepine site of GABAA receptors.