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2-(Ethylsulfanyl)ethyl acetate is an organic compound with the chemical formula C6H12O2S. It is a colorless liquid with a distinctive odor and is soluble in most organic solvents. 2-(ethylsulfanyl)ethyl acetate is primarily used as a synthetic intermediate in the production of various chemicals, including pharmaceuticals, agrochemicals, and fragrances. It is also known as 2-(ethylthio)ethyl acetate or 2-ethylsulfanylethyl acetate. The molecule consists of an ethylsulfanyl group (-SCH2CH3) attached to an ethyl group (-CH2CH3), which is further connected to an acetate group (-COOCH3). Due to its versatile chemical structure, 2-(ethylsulfanyl)ethyl acetate plays a significant role in the synthesis of various target molecules, making it an important building block in the chemical industry.

5862-48-6

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5862-48-6 Usage

Compound type

Ester

Structural description

Ethylsulfanyl group attached to the ethyl group of ethyl acetate

Usage

Solvent in various industries (e.g. coatings, adhesives, pharmaceuticals), fragrance ingredient in perfumes and personal care products

Scent

Fruity and sulfurous

Toxicity

Low toxicity, generally safe for use in commercial products

Check Digit Verification of cas no

The CAS Registry Mumber 5862-48-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5862-48:
(6*5)+(5*8)+(4*6)+(3*2)+(2*4)+(1*8)=116
116 % 10 = 6
So 5862-48-6 is a valid CAS Registry Number.

5862-48-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylsulfanylethyl acetate

1.2 Other means of identification

Product number -
Other names acetic acid-(2-ethylsulfanyl-ethyl 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:5862-48-6 SDS

5862-48-6Downstream Products

5862-48-6Relevant academic research and scientific papers

A facile and efficient method for the reduction of sulfoxides into sulfides with an Al-NiCl2·6H2O system

Raju, B. Rama,Devi, Gitali,Nongpluh, Yoofisaca S.,Saikia, Anil K.

, p. 358 - 360 (2007/10/03)

It has been observed that alkyl aryl and dialkyl sulfoxides can be conveniently and rapidly converted to the corresponding sulfides with an Al-NiCl2-6H2O system in high yields. Ketones are not affected under these reaction conditions.

HOMOLYTIC ADDITION OF 1,3-OXATHIOLANE TO UNSATURATED HYDROCARBONS

Nikolaeva, S. V.,Zorin, V. V.,Zlotskii, S. S.,Rakhmankulov, D. L.

, p. 210 - 214 (2007/10/02)

The homolytic addition of 1,3-oxathiolane to olefins takes place with the formation of 2-substituted 1,3-oxathiolanes and insignificant amounts of functional derivatives of sulfides.

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