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874809-42-4

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874809-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874809-42-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,8,0 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 874809-42:
(8*8)+(7*7)+(6*4)+(5*8)+(4*0)+(3*9)+(2*4)+(1*2)=214
214 % 10 = 4
So 874809-42-4 is a valid CAS Registry Number.

874809-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-[4-(2-cyclopropylmethoxy ethyl)phenoxymethyl]oxirane

1.2 Other means of identification

Product number -
Other names (S)-2-[4-(2-cyclopropylmethoxyethyl)phenoxymethyl]oxirane

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:874809-42-4 SDS

874809-42-4Downstream Products

874809-42-4Relevant articles and documents

Concise synthesis of β-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution

Muthukrishnan,Garud, Dinesh R.,Joshi,Joshi

, p. 1872 - 1876 (2007/10/03)

Enantiopure (S)-metoprolol and (S)-betaxolol were prepared in an extremely simple and practical way using Jacobsen's hydrolytic kinetic resolution of terminal epoxides in isopropanol.

A convenient synthesis of the enantiomerically pure β-blocker (S)-betaxolol using hydrolytic kinetic resolution

Joshi, Ramesh A.,Garud, Dinesh R.,Muthukrishnan,Joshi, Rohini R.,Gurjar

, p. 3802 - 3806 (2007/10/03)

Enantiopure (S)-betaxolol was prepared in an extremely simple and practical way using hydrolytic kinetic resolution of a terminal epoxide by Jacobsen's catalyst. High enantiomeric purity (99% ee) has been achieved and the method is amenable to industrial scale-up.

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