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Thioacetic acid S-undecyl ester, also known as undecyl thioacetate, is an organic compound with the chemical formula C13H26OS. It is a colorless liquid that is soluble in organic solvents and has a slight, characteristic odor. This ester is formed by the reaction of thioacetic acid with undecanol, and it is used as a synthetic intermediate in the preparation of various organic compounds, including pharmaceuticals, agrochemicals, and fragrances. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry.

2432-35-1

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2432-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2432-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2432-35:
(6*2)+(5*4)+(4*3)+(3*2)+(2*3)+(1*5)=61
61 % 10 = 1
So 2432-35-1 is a valid CAS Registry Number.

2432-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name S-undecyl ethanethioate

1.2 Other means of identification

Product number -
Other names Undecyl-thioacetat

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:2432-35-1 SDS

2432-35-1Relevant academic research and scientific papers

A novel tin-free procedure for alkyl radical reactions

Benati, Luisa,Leardini, Rino,Minozzi, Matteo,Nanni, Daniele,Scialpi, Rosanna,Spagnolo, Piero,Strazzari, Samantha,Zanardi, Giuseppe

, p. 3598 - 3601 (2007/10/03)

Desulfuration as a source of alkyl radicals: The addition of alkylsulfanyl radicals to isocyanides gives the corresponding alkyl radicals. This methodology can replace the usual tin-mediated radical procedures and allows for the generation of tertiary, secondary, and even nonstabilized primary radicals that can be used efficiently in reductive defunctionalizations and intermolecular additions to electron-rich olefins (see scheme).

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