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105183-42-4

105183-42-4

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105183-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105183-42-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,1,8 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 105183-42:
(8*1)+(7*0)+(6*5)+(5*1)+(4*8)+(3*3)+(2*4)+(1*2)=94
94 % 10 = 4
So 105183-42-4 is a valid CAS Registry Number.

105183-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetic acid (R)-1-acetoxymethyl-2-(benzyl-isopropyl-amino)-ethyl ester

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:105183-42-4 SDS

105183-42-4Downstream Products

105183-42-4Relevant articles and documents

Synthesis of novel and enantiomerically pure epoxypropylamine: A divergent route to the chiral β-adrenergic blocking agents

Hou, Xue-Long,Li, Bin-Feng,Dai, Li-Xin

, p. 2319 - 2326 (2007/10/03)

The chiral building block (S)-N-benzyl-N-isopropyl-2,3-epoxypropylamine is obtained by means of chlorohydroxylation of allylamine, followed by Jacobsen's hydrolytic kinetic resolution with water. A concise, divergent five-step synthesis of three β-adrenergic blocking agents in high enantiomeric excess using (S)-N-benzyl-N-isopropyl-2,3-epoxypropylamine as the key intermediate is described.

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