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895367-63-2

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895367-63-2 Usage

General Description

2-CHLORO-N-(2-FLUOROBENZYL)ACETAMIDE is a chemical compound with the molecular formula C9H9ClFNO. It is a chloro-substituted acetamide derivative with a fluorobenzyl group. 2-CHLORO-N-(2-FLUOROBENZYL)ACETAMIDE is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in research and development for the production of new chemical compounds. 2-CHLORO-N-(2-FLUOROBENZYL)ACETAMIDE may have potential applications in the field of medicinal chemistry, particularly in the development of new drugs for various therapeutic purposes. Due to its chemical structure and properties, it is important to handle this compound with care and in accordance with safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 895367-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,3,6 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 895367-63:
(8*8)+(7*9)+(6*5)+(5*3)+(4*6)+(3*7)+(2*6)+(1*3)=232
232 % 10 = 2
So 895367-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H9ClFNO/c10-5-9(13)12-6-7-3-1-2-4-8(7)11/h1-4H,5-6H2,(H,12,13)

895367-63-2SDS

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 2-Chloro-N-(2-fluorobenzyl)acetamide

1.2 Other means of identification

Product number -
Other names 2-chloro-N-[(2-fluorophenyl)methyl]acetamide

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:895367-63-2 SDS

895367-63-2Downstream Products

895367-63-2Relevant articles and documents

Lanthanide Complexes that Respond to Changes in Cyanide Concentration in Water

Routledge, Jack D.,Zhang, Xuejian,Connolly, Michael,Tropiano, Manuel,Blackburn, Octavia A.,Kenwright, Alan M.,Beer, Paul D.,Aldridge, Simon,Faulkner, Stephen

, (2017)

Cyanide ions are shown to interact with lanthanide complexes of phenacylDO3A derivatives in aqueous solution, giving rise to changes in the luminescence and NMR spectra. These changes are the consequence of cyanohydrin formation, which is favored by the c

Probing structural requirements of positive allosteric modulators of the M4 muscarinic receptor

Huynh, Tracey,Valant, Celine,Crosby, Ian T.,Sexton, Patrick M.,Christopoulos, Arthur,Capuano, Ben

, p. 8196 - 8200 (2013/11/06)

The M4 mAChR is implicated in several CNS disorders and possesses an allosteric binding site for which ligands modulating the affinity and/or efficacy of ACh may be exploited for selective receptor targeting. We report the synthesis of a focused library of putative M4 PAMs derived from VU0152100 and VU10005. These compounds investigate the pharmacological effects of previously identified methoxy and fluoro substituents, providing useful estimates of affinity (KB), cooperativity (αβ), and direct agonist properties (τB).

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