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38425-59-1

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38425-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38425-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38425-59:
(7*3)+(6*8)+(5*4)+(4*2)+(3*5)+(2*5)+(1*9)=131
131 % 10 = 1
So 38425-59-1 is a valid CAS Registry Number.

38425-59-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzoic acid,1-ethoxyethenol

1.2 Other means of identification

Product number -
Other names Ethenol,1-ethoxy-,benzoate

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:38425-59-1 SDS

38425-59-1Relevant articles and documents

Silver-catalyzed regio- and stereoselective addition of carboxylic acids to ynol ethers

Yin, Jing,Bai, Yihui,Mao, Mengyi,Zhu, Gangguo

, p. 9179 - 9185 (2015/02/19)

A silver-catalyzed trans addition of carboxylic acids to ynol ethers is described. The reaction has a broad scope with respect to carboxylic acids and ynol ethers, delivering (Z)-α-alkoxy enol esters in good yields with excellent regio- and stereoselectiv

Enzyme-catalyzed asymmetrization of 2,2-disubstituted 1,3-propanediols using 1-ethoxyvinyl esters

Akai, Shuji,Naka, Tadaatsu,Takebe, Yasushi,Kita, Yasuyuki

, p. 4243 - 4246 (2007/10/03)

The lipase-catalyzed asymmetrization of the prochiral 2,2-disubstituted 1,3-propanediols 1, 6, and 9 was studied using various types of 1-ethoxyvinyl esters 2. Among them, the use of the benzoate 2f provided good chemical and optical yields of the products 3, 7, and 10 bearing chiral quaternary carbon centers which are fairly stable against racemization.

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