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3-Cyclohexene-1,2-diol, 2-phenyl-, 1-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

674309-48-9

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674309-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 674309-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,4,3,0 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 674309-48:
(8*6)+(7*7)+(6*4)+(5*3)+(4*0)+(3*9)+(2*4)+(1*8)=179
179 % 10 = 9
So 674309-48-9 is a valid CAS Registry Number.

674309-48-9SDS

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 2-phenyl-3-cyclohexene-1,2-diol

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:674309-48-9 SDS

674309-48-9Relevant academic research and scientific papers

Influence of Michael acceptor stereochemistry on intramolecular Morita-Baylis-Hillman reactions

Teng, Wen-Dong,Huang, Rui,Kwong, Cathy Kar-Wing,Shi, Min,Toy, Patrick H.

, p. 368 - 371 (2007/10/03)

A study of the effect of Michael acceptor stereochemistry on the efficiency of intramolecular Morita-Baylis-Hillman (MBH) reactions has been performed. The reactions were catalyzed by a phosphine, and the reaction substrates studied were enones containing

The intramolecular Baylis-Hillman reaction: Easy preparation of versatile substrates, facile reactions, and synthetic applications

Yeo, Jung Eun,Yang, Xiuling,Kim, Hee Jin,Koo, Sangho

, p. 236 - 237 (2007/10/03)

We have developed a general and highly efficient method for the preparation of diverse ω-formyl-aα,β-unsaturated carbonyl compounds and optimized the conditions for the intramolecular Baylis-Hillman reactions of these compounds to provide various biologic

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