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682-11-1

682-11-1

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682-11-1 Usage

Chemical Properties

CLEAR COLOURLESS VISCOUS LIQUID

Check Digit Verification of cas no

The CAS Registry Mumber 682-11-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 682-11:
(5*6)+(4*8)+(3*2)+(2*1)+(1*1)=71
71 % 10 = 1
So 682-11-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O3/c1-4-6-12-7-9(3,5-2)8(10)11/h4,8,10-11H,1,5-7H2,2-3H3

682-11-1 Well-known Company Product Price

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  • Aldrich

  • (416118)  Trimethylolpropaneallylether  98%

  • 682-11-1

  • 416118-500ML

  • 713.70CNY

  • Detail

682-11-1SDS

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 2-ethyl-2-(prop-2-enoxymethyl)propane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2-(allyloxymethyl)-2-ethyl-1,3-propane diolbutanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:682-11-1 SDS

682-11-1Relevant articles and documents

Selective functionalization of the primary hydroxy group in triols

Raskil'Dina,Valiev,Sultanova,Zlotskii

, p. 1599 - 1604 (2016/02/18)

A procedure was suggested for preparing functionally substituted 1,2-diols by O-alkylation of hydroxyalkyl-1,3-dioxacyclanes with alkyl halides, followed by acid hydrolysis. The conditions for selective cleavage of the ethers obtained were found. (2,2-Dimethyl-1,3-dioxolan-4-yl)methyl benzoate under the conditions of acid deacetalization undergoes saponification of the ester group.

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