881844-11-7

Basic information

• Product Name: 4-chloro-1-(4-Methoxybenzyl)-1H-iMidazo[4,5-c]pyridine
• Synonyms: 4-chloro-1-(4-Methoxybenzyl)-1H-iMidazo[4,5-c]pyridine;4-chloro-1-(4-Methoxybenzyl)-1H-iMidazo[4,5-c]pyridine-5
• CAS NO: 881844-11-7
• Molecular Formula: C₁₄H₁₂ClN₃O
• Molecular Weight: 273.71758
• Mol File: 881844-11-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 483.0±55.0 °C(Predicted)
• Appearance: /
• Density: 1.31±0.1 g/cm3(Predicted)
• PKA: 3.11±0.30(Predicted)
• CAS DataBase Reference: 4-chloro-1-(4-Methoxybenzyl)-1H-iMidazo[4,5-c]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-1-(4-Methoxybenzyl)-1H-iMidazo[4,5-c]pyridine(881844-11-7)
• EPA Substance Registry System: 4-chloro-1-(4-Methoxybenzyl)-1H-iMidazo[4,5-c]pyridine(881844-11-7)

Safety Data

• Hazardous Substances Data: 881844-11-7(Hazardous Substances Data)

Usage

General Description

4-chloro-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridine is a chemical compound with a molecular formula C15H14ClN3O. It is a heterocyclic organic compound that contains a chlorine atom, a methoxybenzyl group, and an imidazopyridine ring system. 4-chloro-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridine may be used in the pharmaceutical industry for the development of new drugs due to its potential therapeutic properties. It may also be used in research and development in the fields of medicine and biochemistry. Additionally, it is important to handle this chemical with care and follow proper safety precautions due to its potential hazards if used improperly. Overall, 4-chloro-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridine is a versatile compound with potential applications in various industries.

Upstream product

• 2770-01-6 4-chloro-1H-imidazo[4,5-c]pyridine 
• 824-94-2 p-methoxybenzyl chloride 
• 39217-08-8 2-chloropyridine-3,4-diamine 
• 2789-25-5 2-chloro-3-nitropyridin-4-amine 
• 14432-12-3 4-Amino-2-chloropyridine 
• 14432-16-7 2-chloro-4-nitropyridine-N-oxide 
• 2402-95-1 2-chloropyridine-N-oxide 
• 109-09-1 2-chloropyridine 
• 881844-10-6 2-chloro-N⁴-(4-methoxybenzyl)pyridine-3,4-diamine 
• 122-51-0 orthoformic acid triethyl ester 
• 5975-12-2 2,4-dichloro-3-nitro-pyridine 
• 89282-12-2 2,4-dihydroxy-3-nitropyridine 
• 881844-09-3 2-chloro-N-(4-methoxybenzyl)-3-nitropyridin-4-amine 

Downstream Products

• 1313714-36-1 4-(furan-2-yl)-1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridine 
• 6811-77-4 3-deazaadenine 
• 881844-18-4 4-amino-3-[2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-7-nitro-3H-imidazo[4,5-c]pyridine 
• 881844-13-9 4-amino-1-[2'-deoxy-3',5'-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-7-nitro-1H-imidazo[4,5-c]pyridine 
• 881844-12-8 4-(isobutyrylamino)-1H-imidazo[4,5-c]pyridine 
• 3243-26-3 4-hydrazino-1H-imidazo[4,5-c]pyridine 

Relevant articles and documents

Design and synthesis of purine analogues as highly specific ligands for FcyB, a ubiquitous fungal nucleobase transporter

In the course of our study on fungal purine transporters, a number of new 3-deazapurine analogues have been rationally designed, based on the interaction of purine substrates with the Aspergillus nidulans FcyB carrier, and synthesized following an effective synthetic procedure. Certain derivatives have been found to specifically inhibit FcyB-mediated [3H]-adenine uptake. Molecular simulations have been performed, suggesting that all active compounds interact with FcyB through the formation of hydrogen bonds with Asn163, while the insertion of hydrophobic fragments at position 9 and N6 of 3-deazaadenine enhanced the inhibition.