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1,2-Decanediol, diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60671-14-9

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60671-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60671-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,6,7 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60671-14:
(7*6)+(6*0)+(5*6)+(4*7)+(3*1)+(2*1)+(1*4)=109
109 % 10 = 9
So 60671-14-9 is a valid CAS Registry Number.

60671-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,decane-1,2-diol

1.2 Other means of identification

Product number -
Other names acetic acid 2-acetoxy-decyl 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:60671-14-9 SDS

60671-14-9Relevant academic research and scientific papers

ALKENE OXIDATION BY AN IRON(II)/PERSULFATE/ACETIC ACID SYSTEM

Fristad, William E.,Peterson, John R.

, p. 1469 - 1476 (2007/10/02)

Mono- and disubstituted alkenes were converted to trans-vicinal diacetates by heating with an iron(II)/persulfate/acetic acid system.The synthetic utility and limitations were identified.A mechanism for the transformation is proposed wich involves an initial addition of sulfate radical anion to the alkene followed by solvolysis, addition, hydrolysis, and acetylation.

IRON(II) CATALYZED ODIDATION OF ALKENES TO VICINAL DIACETATES

Fristad, William E.,Peterson, John R.

, p. 4547 - 4550 (2007/10/02)

Mono- and disubstituted alkenes are converted to trans-vicinal diacetates by heating with an acetic acid solution of ammonium persulfate and a ferrous sulfate catalyst.

The Deoxygenation of NN-Dialkylaminothiocarbonyloxyalkanes

Barrett, Anthony G. M.,Prokopiou, Panayiotis A.,Barton, Derek H. R.

, p. 1510 - 1516 (2007/10/02)

The title compounds were converted into alkanes in high yield on reduction with potassium and 18-crown-6 in t-butylamine.Thereby both primary and secondary alcohols were conveniently deoxygenated.

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