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21535-43-3

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21535-43-3 Usage

Chemical Properties

Light Brown Solid

Uses

2-Chloro-N-[2-(benzyl)phenyl]acetamide (cas# 21535-43-3) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 21535-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,3 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21535-43:
(7*2)+(6*1)+(5*5)+(4*3)+(3*5)+(2*4)+(1*3)=83
83 % 10 = 3
So 21535-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H14ClNO/c16-11-15(18)17-14-9-5-4-8-13(14)10-12-6-2-1-3-7-12/h1-9H,10-11H2,(H,17,18)

21535-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-benzylphenyl)-2-chloroacetamide

1.2 Other means of identification

Product number -
Other names 2-Chloro-|A-phenyl-o-acetotoluidide

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:21535-43-3 SDS

21535-43-3Relevant articles and documents

Novel method of preparing Epinastine

-

Paragraph 0071-0074, (2020/05/13)

The present invention relates to a novel manufacturing method for synthesizing an anti-histamine pharmaceutical medicine, epinastine. The novel manufacturing method for synthesizing epinastine according to the present invention has fewer synthesizing steps than a conventional epinastine manufacturing method, and is a safe synthesis method, thereby being expected to be used for inexpensively synthesizing the anti-histamine pharmaceutical medicine, epinastine by the manufacturing method, and supplying the same to the market.COPYRIGHT KIPO 2020

Stereoselective synthesis of (R)-(-)-mianserin

Pawlowska,Czarnocki,Wojtasiewicz,Maurin

, p. 3335 - 3342 (2007/10/03)

(14bR)-2-Methyl-1,2,3,4,10,14b-hexahydrodibenzo[c,f]pyrazino[1,2-a]azepine, (R)-(-)-mianserin 1a was synthesised in several steps in good enantiomeric purity with the use of (S)-(-)-α-methylbenzylamine 5. The absolute configuration was assigned on the bas

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