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Heptanethioic acid S-methyl ester, with the molecular formula C8H18OS, is a colorless to pale yellow liquid characterized by a strong sulfur-like odor. This chemical compound is known for its stability under normal conditions, although it requires careful handling due to its potential violent reactions with oxidizing agents and strong acids.

2432-82-8

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2432-82-8 Usage

Uses

Used in the Food Industry:
Heptanethioic acid S-methyl ester is used as a flavoring agent for enhancing the taste and aroma of various food products, contributing to a more appealing sensory experience for consumers.
Used in the Cosmetic and Perfume Industries:
In these industries, Heptanethioic acid S-methyl ester serves as a fragrance additive, providing unique and desirable scents to a range of cosmetic and perfume products, thereby increasing their marketability and consumer appeal.
Used in the Chemical Synthesis Industry:
Heptanethioic acid S-methyl ester is utilized as an intermediate in the synthesis of other organic compounds, playing a crucial role in the production of various chemical products and contributing to the advancement of the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 2432-82-8 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, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2432-82:
(6*2)+(5*4)+(4*3)+(3*2)+(2*8)+(1*2)=68
68 % 10 = 8
So 2432-82-8 is a valid CAS Registry Number.

2432-82-8SDS

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-Methylheptanthionat

1.2 Other means of identification

Product number -
Other names Methyl-thioheptanoat

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:2432-82-8 SDS

2432-82-8Downstream Products

2432-82-8Relevant academic research and scientific papers

THIOALKYLTRIBUTYL- AND THIOALKOXYTRIPHENYLPHOSPHONIUM SALTS: PREPARATION AND APPLICATION TO THE SYNTHESIS OF THIOLESTERS AND UNSYMMETRICAL SULFIDES

Ohmori, Hidenobu,Maeda, Hatsuo,Konomoto, Kohichi,Sakai, Kiyoshi,Masui, Masaichiro

, p. 4473 - 4481 (2007/10/02)

Thioalkoxyphosphonium salts, Ph3PSR(1+)*ClO4(1-) (3) and Bu3PSR(1+)*X(1-) (X=ClO4 and BF4) (5), have been prepared from the corresponding tertiary phosphines and disulfides by simple procedures, which involve (i) constant current electrolysis in acetonitrile in the presence of either HClO4 (for 3) or PhCOOH and LiX (for 5), and (ii) stirring an equimolar mixture of a phosphine, a disulfide, PHCOOH, and LiX in acetonitrile at ambient temperature.For the preparation of 3, which have been reported as useful reagents for the synthesis of unsymmetrical disulfides, the electrochemical method is recomended, while for 5 the latter non-electrochemicl procedure gave better results.Reactions of the phosphonium salts 5 with carboxylic acidsand primary alcohols in benzene at ambient temperature gave thiolesters and unsymmetrical sulfides, respectively, in fair to excellent yields.Keywords - triphenylphosphine; tributylphosphine; disulfide; thioalkoxyphosphonium salt; thiolester; unsymmetrical sulfide

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