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Hexanethioic acid S-heptyl ester, also known as 1-hexanethiol heptyl ester or hexyl heptyl sulfide, is an organic compound with the chemical formula C13H28S. It is a colorless liquid with a strong, unpleasant odor. Hexanethioic acid S-heptyl ester is formed by the esterification of hexanethioic acid (a sulfur analog of carboxylic acids) with heptanol. It is used in the synthesis of various organic compounds and as a chemical intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its low toxicity and relatively stable nature, hexanethioic acid S-heptyl ester is considered a valuable building block in the chemical industry.

2432-80-6

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2432-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2432-80-6 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 2432-80:
(6*2)+(5*4)+(4*3)+(3*2)+(2*8)+(1*0)=66
66 % 10 = 6
So 2432-80-6 is a valid CAS Registry Number.

2432-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Heptyl-thiohexanoat

1.2 Other means of identification

Product number -
Other names Hexanethioic acid S-heptyl 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:2432-80-6 SDS

2432-80-6Downstream Products

2432-80-6Relevant academic research and scientific papers

Tandem Acyl Substitution/Michael Addition of Thioesters with Vinylmagnesium Bromide

Hirschbeck, Vera,B?ldl, Marlene,Gehrtz, Paul H.,Fleischer, Ivana

, p. 2578 - 2582 (2019)

A tandem reaction of thioesters with vinylmagnesium bromide is reported. The initial acyl substitution provides an α,β-unsaturated ketone which further reacts with the liberated thiolate. This transition-metal-free synthesis of β-sulfanyl ketones takes place under mild reaction conditions, whereas the addition of a second Grignard molecule is almost completely suppressed. The carefully chosen parameters enabled the transformation of different substrates in moderate to good yields.

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