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Acetamide, N-(2-benzoyl-4-chlorophenyl)-2-[(2-hydroxy-1-phenylethyl)amino]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126517-41-7

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126517-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126517-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,5,1 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126517-41:
(8*1)+(7*2)+(6*6)+(5*5)+(4*1)+(3*7)+(2*4)+(1*1)=117
117 % 10 = 7
So 126517-41-7 is a valid CAS Registry Number.

126517-41-7SDS

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 D(+)-N-(2-Benzoyl-4-chlorophenyl)-2-(2-hydroxy-1-phenylethylamino)acetamide

1.2 Other means of identification

Product number -
Other names N-(2-Benzoyl-4-chloro-phenyl)-2-(2-hydroxy-1-phenyl-ethylamino)-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:126517-41-7 SDS

126517-41-7Downstream Products

126517-41-7Relevant academic research and scientific papers

POTENTIAL ANTICONVULSANTS: 3-CHLOROBENZOPHENONE DERIVATIVES

Jilek, Jiri,Urban, Jiri,Kmonicek, Vojtech,Pomykacek, Josef,Holubek, Jiri,et al.

, p. 2248 - 2260 (2007/10/02)

Reactions of 2-(2-iodoacetamido)-5-chlorobenzophenone with 2-amino-2-phenylethanol, 2-amino-1-phenylethanol, 3-amino-2-phenylpropanol, D(+)-norpseudoephedrine, and 2-aminopropane-2-carbonitrile gave the 2-substituted N-(2-benzoyl-4-chlorophenyl)acetamides X-XIV. 2,3'-Dichlorobenzhydrol (XVI) and 2,3'-dichlorobenzhydryl chloride (XIX) were transformed to the ethers XVII and XVIII and to the amines XXI-XXIV.Compound XVI was oxidized to the ketone XXV which was transformed via the oxime XXVI to compound XXVII.The basic products were converted to salts which were pharmacologically tested.Compounds X, XVII, XXIII, and XXVII showed anticonvulsant effects and some other neurotropic activities.

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