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Essigsaeureethoxy(dithioameisensaeure)anhydrid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79598-15-5

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79598-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79598-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,9 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79598-15:
(7*7)+(6*9)+(5*5)+(4*9)+(3*8)+(2*1)+(1*5)=195
195 % 10 = 5
So 79598-15-5 is a valid CAS Registry Number.

79598-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Essigsaeureethoxy(dithioameisensaeure)anhydrid

1.2 Other means of identification

Product number -
Other names S-(acetyl)-O-ethyldithiocarbonate

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:79598-15-5 SDS

79598-15-5Relevant academic research and scientific papers

PYROTHIOCARBONATES V. SYNTHESIS AND SOME REACTIONS OF S-TRIMETHYLSILYL O-ALKYLDITHIOCARBONATES

Palominos, Mario A.,Vega, Juan C.

, p. 319 - 324 (2007/10/02)

Non-reported S-trimethylsilyl-O-alkyldithiocarbonates (2) are prepared by reaction of O,O-dialkyltrithiodicarbonates with N-methyl-N-trimethylsilylaniline in 87-96percent yield.These air-sensitive liquids which are separated from accompanying phenyl methyl alkylcarbamothioates by fractional distillation.The reaction of 2 with acetyl chloride gives the unsymmetrical dithioanhydrides S-acetyl O-alkyldithiocarbonates in 93-97percent yield.With the less powerfull electrophilic reagent, iodomethane, S-trimethylsilyl O-ethyldithiocarbonate (2a) forms S-methyl O-ethyldithiocarbonate in 30percent yield.When a chloroform solution of 2a is stirred with water the unstable compound O-ethyldithiocarbonic acid is obtained. Key words: Masked O-alkyldithiocarbonic acids; O,O-dialkyltrithiodicarbonates; S-acetyl O-alkyl-dithiocarbonates.

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