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302571-77-3

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302571-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302571-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,5,7 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 302571-77:
(8*3)+(7*0)+(6*2)+(5*5)+(4*7)+(3*1)+(2*7)+(1*7)=113
113 % 10 = 3
So 302571-77-3 is a valid CAS Registry Number.

302571-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-N,N-diethyl-3-hydroxy-3-phenylpropanamide

1.2 Other means of identification

Product number -
Other names 2-chloro-3-hydroxy-3-phenyl-propionic acid diethylamide

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:302571-77-3 SDS

302571-77-3Relevant articles and documents

Synthesis of Aromatic (E)- or (Z)-α,β-Unsaturated Amides with Total or Very High Selectivity from α,β-Epoxyamides and Samarium Diiodide

Concellon, Jose M.,Bardales, Eva

, p. 9492 - 9495 (2007/10/03)

Highly stereoselective synthesis of aromatic α,β-unsaturated amides was achieved by treatment of aromatic α,β-epoxyamides with samarium diiodide. The starting compounds 1 and 3 are easily prepared by the reaction of enolates derived from α-chloroamides wi

Synthesis of (E)-α,β-unsaturated amides with high selectivity by using samarium diiodide

Concellon, Jose M.,Perez-Andres, Juan A.,Rodriguez-Solla, Humberto

, p. 3062 - 3068 (2007/10/03)

Stereoselective β-elimination of 2-chloro-3-hydroxyamides 1 is achieved by using samarium diiodide to yield α,β-unsaturated amides 2, in which the C=C bond is di- tri-, or tetrasubstituted. The starting compounds 1 are easily prepared by reaction of the c

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