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Methylhexadecyl sulfoxide, also known as 1-hexadecanethiol methyl sulfoxide, is an organic compound with the chemical formula C17H36OS. It is a colorless to pale yellow liquid with a mild, sulfur-like odor. Methylhexadecyl sulfoxide is characterized by its unique sulfur-oxygen (S-O) bond, which is responsible for its distinct chemical properties. Methylhexadecyl sulfoxide is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a reagent in organic synthesis, where its sulfur-oxygen bond can be exploited for various transformations. Due to its reactive nature, it is essential to handle Methylhexadecyl sulfoxide with care, following proper safety protocols.

3079-32-1

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3079-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3079-32-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3079-32:
(6*3)+(5*0)+(4*7)+(3*9)+(2*3)+(1*2)=81
81 % 10 = 1
So 3079-32-1 is a valid CAS Registry Number.

3079-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl n-hexadecyl sulfoxide

1.2 Other means of identification

Product number -
Other names 1-Methanesulfinyl-hexadecane

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:3079-32-1 SDS

3079-32-1Downstream Products

3079-32-1Relevant academic research and scientific papers

β-Sulfinyl acrylate esters as a convenient source of alkane- and arenesulfenate anions

O'Donnell, Jennifer S.,Schwan, Adrian L.

, p. 6293 - 6296 (2007/10/03)

Methyl acrylate esters bearing alkane- and arenesulfinyl units on the 2-carbon liberate sulfenate anions upon nucleophilic attack. The sulfenates are readily captured through sulfur alkylation. When a sulfenate derived from R-cysteine is generated, diastereoselective benzylation is observed.

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