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(S)-4-Hydroxy-3,5,5-trimethyl-4-(toluene-4-sulfonylmethyl)-cyclohex-2-enone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

518316-69-3

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518316-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 518316-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,8,3,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 518316-69:
(8*5)+(7*1)+(6*8)+(5*3)+(4*1)+(3*6)+(2*6)+(1*9)=153
153 % 10 = 3
So 518316-69-3 is a valid CAS Registry Number.

518316-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-4-hydroxy-3,5,5-trimethyl-4-(tosylmethyl)cyclohex-2-en-1-one

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:518316-69-3 SDS

518316-69-3Upstream product

518316-69-3Relevant academic research and scientific papers

β-hydroxysulfoxides as chiral cyclic ketone equivalents: Enantioselective synthesis of polysubstituted cyclohexanones, cyclohexenones and cyclohexenediones

Carreno, M. Carmen,Perez-Gonzalez, Manuel,Ribagorda, Maria,Somoza, Alvaro,Urbano, Antonio

, p. 3052 - 3053 (2007/10/03)

The β-hydroxysulfoxide moiety, after oxidation to sulfone, acts as a masked carbonyl group in a cyclic system, opening an easy access to differently substituted enantiomerically pure cyclic ketones by means of aluminium-mediated conjugate additions, stereoselective reductions and elimination by retrocondensation in basic medium.

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