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52790-15-5

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52790-15-5 Usage

General Description

ETHYL 2-[(ETHOXYCARBONYL)THIO]ACETATE, also known by its chemical formula C9H16O4S, is a compound used in organic synthesis. It is characterized by its ethyl ester and thioester functional groups, making it suitable for use as an intermediate in the production of pharmaceuticals, pesticides, and other fine chemicals. ETHYL 2-[(ETHOXYCARBONYL)THIO]ACETATE has a mild, fruity odor and is commonly used as a flavoring agent in the food industry. It is typically synthesized by reacting ethyl 2-bromoacetate with potassium thioacetate in the presence of a base, resulting in the formation of the desired product through an S-alkylation reaction. Its key properties make it a valuable building block for a wide range of chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 52790-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52790-15:
(7*5)+(6*2)+(5*7)+(4*9)+(3*0)+(2*1)+(1*5)=125
125 % 10 = 5
So 52790-15-5 is a valid CAS Registry Number.

52790-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-ethoxycarbonylsulfanylacetate

1.2 Other means of identification

Product number -
Other names Ethyl [(Ethoxycarbonyl)thio]acetate

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:52790-15-5 SDS

52790-15-5Relevant articles and documents

Reactions of Dithiocarbamates and Thiocarbonates with Heterocumulenes

Doelling, Wolfgang,Sperk, Katrin,Augustin, Manfred

, p. 671 - 678 (2007/10/02)

3,3-Bis(alkylthio)-2-dialkylaminothiocarbonylthioacrylonitriles 3-5 are obtained by dithiocarboxylation reaction of N,N-disubstituted S-cyanomethyl dithiocarbamates 1a-c in NaH/THF at -15 deg C followed by alkylation.Treatment of N,N-dimethyl-S-methylthiomethyldithiocarbamate 6 with CS2/2 n-BuLi in THF at -55 deg C gives N,N-dimethyl S-dithiocarbamates 7a-c.Phenylisothiocyanat reacts with S-alkoxycarbonylmethyl-O-alkylthiocarbonates 8a, b in the presence of t-BuOK/dry DMF to yield 4-subst. 2-oxo-3-phenyl-1,3-thiazoline-5-carboxylates 11a-e.

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