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56643-69-7

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56643-69-7 Usage

Structure

A derivative of imidazole with a chlorophenylmethyl group attached to the imidazole ring

Usage

Commonly used in pharmaceutical and medicinal applications as a building block for the synthesis of biologically active molecules

Potential applications

May have potential in the field of organic chemistry for the development of new synthetic methodologies

Biological activities

May exhibit certain biological activities or pharmacological properties useful for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 56643-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56643-69:
(7*5)+(6*6)+(5*6)+(4*4)+(3*3)+(2*6)+(1*9)=147
147 % 10 = 7
So 56643-69-7 is a valid CAS Registry Number.

56643-69-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-chlorophenyl)methyl]imidazole

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56643-69-7 SDS

56643-69-7Relevant articles and documents

Synthesis and investigation of inhibitory activities of imidazole derivatives against the metallo-β-lactamase IMP-1

Khalili Arjomandi, Omid,Kavoosi, Mahboubeh,Adibi, Hadi

, (2019/09/19)

Mutations in bacteria can result in antibiotic resistance due to the overuse or abuse of β-lactam antibiotics. One strategy which bacteria can become resistance toward antibiotics is secreting of metallo β-lactamase enzymes that can open the lactam ring of the β-lactam antibiotic and inactivate them. This issue is a threat for human health and one strategy to overcome this situation is co-administration of β-lactam antibiotics with an inhibitor. So far, no clinically available inhibitors of metallo β-lactamases (MBLs) reported and the clinically inhibitors of serine β-lactamase are useless for MBLs. Accordingly, finding a potent inhibitor of the MBLs being very important. In this study, imidazole derivatives primarily were synthesized and their inhibitory activity were measured. Later in silico binding model was used to predict the configuration and conformation of the ligands into the active site of enzyme. Two molecules demonstrated with IC50 of 39 μM and 46 μM against MBL (IMP-1).

Substituted 5-(alkyl)carboxamide imidazoles

-

, (2008/06/13)

Angiotensin II receptor antagonists having the formula: STR1 which are useful in regulating hypertension and in the treatment of congestive heart failure, renal failure, and glaucoma pharmaceutical compositions including these antagonists, and methods of

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