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3-Cyclohexen-1-one, 3-(acetyloxy)-2-methyl-2-(2-propenyl)-, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153563-93-0

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153563-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153563-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,5,6 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153563-93:
(8*1)+(7*5)+(6*3)+(5*5)+(4*6)+(3*3)+(2*9)+(1*3)=140
140 % 10 = 0
So 153563-93-0 is a valid CAS Registry Number.

153563-93-0SDS

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 (+)-(S)-3-Acetoxy-2-methyl-2-(prop-2-enyl)cyclohex-3-enone

1.2 Other means of identification

Product number -
Other names Acetic acid (S)-6-allyl-6-methyl-5-oxo-cyclohex-1-enyl ester

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:153563-93-0 SDS

153563-93-0Relevant academic research and scientific papers

Asymmetric Synthesis by Enzymatic Hydrolysis of Prochiral Dienol Diacetate.

Duhamel, Pierre,Renouf, Philippe,Cahard, Dominique,Yebga, Albert,Poirier, Jean-Marie

, p. 2447 - 2450 (1993)

Enzymatic hydrolysis of prochiral dienol diacetate 1 by Candida cylindracea lipase (CCL) leads to the keto enol acetate 2 in high yield with an enantiometric excess>98percent.The S configuration of the asymmetric center was assigned.

Asymmetric hydrolysis of pro-chiral 3,3-disubstituted 2,4-diacetoxy-cyclohexa-1,4-dienes

Renouf, Philippe,Poirier, Jean-Marie,Duhamel, Pierre

, p. 1739 - 1745 (2007/10/03)

Asymmetric enzymatic hydrolysis of pro-chiral 3,3-disubstituted 2,4-diacetoxycyclohexa-1,4-dienes 2 affords in high yields optically pure 2,2-disubstituted 3-acetoxycyclohex-3-enones 1 (>98% ee). Under mild conditions Candida cylindracea lipase (enzyme/substrate ratio = 2%) hydrolyses specifically the pro-S enol ester function of the pro-chiral starting material 2.

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