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Benzene, 1-(phenylmethoxy)-4-[2-(2-propenyloxy)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

761449-63-2

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761449-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 761449-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,4 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 761449-63:
(8*7)+(7*6)+(6*1)+(5*4)+(4*4)+(3*9)+(2*6)+(1*3)=182
182 % 10 = 2
So 761449-63-2 is a valid CAS Registry Number.

761449-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-alyloxyethyl)-4-benzyloxybenzene

1.2 Other means of identification

Product number -
Other names 1-(2-allyloxyethyl)-4-benzyloxybenzene

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:761449-63-2 SDS

761449-63-2Relevant academic research and scientific papers

PROCESS FOR PREPARATION OF S-(-)-BETAXOLOL AND SALTS THEREOF

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Page/Page column 2-5, (2010/02/15)

The present invention relates to an improved process for preparation of S-(?)-betaxolol salts. More particularly the present invention relates to the preparation of hydrochloride salt of S-(?)-betaxolol of formula (1).

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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