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Methyl 3-(acetylsulfanyl)propanoate is an organic compound with the chemical formula C6H10O3S. It is a colorless liquid with a fruity odor and is commonly used as a flavoring agent in the food and beverage industry. It is also used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Methyl 3-(acetylsulfanyl)propanoate is known for its sweet, pleasant smell and is often utilized in perfumes and fragrance applications. Additionally, it has been identified as a potential bioactive compound with anti-inflammatory and antimicrobial properties, making it a subject of interest in the field of drug discovery and development.

6291-62-9

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6291-62-9 Usage

Uses

Used in Food and Beverage Industry:
Methyl 3-(acetylsulfanyl)propanoate is used as a flavoring agent for its fruity odor and sweet, pleasant smell, enhancing the taste and aroma of various food and beverage products.
Used in Perfumes and Fragrances:
Methyl 3-(acetylsulfanyl)propanoate is used as a fragrance ingredient for its sweet, pleasant smell, contributing to the creation of various perfumes and fragrances.
Used in Pharmaceutical and Agrochemical Synthesis:
Methyl 3-(acetylsulfanyl)propanoate is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, playing a crucial role in the production of various drugs and agricultural chemicals.
Used in Drug Discovery and Development:
Methyl 3-(acetylsulfanyl)propanoate is used as a potential bioactive compound with anti-inflammatory and antimicrobial properties, making it a subject of interest in the field of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 6291-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6291-62:
(6*6)+(5*2)+(4*9)+(3*1)+(2*6)+(1*2)=99
99 % 10 = 9
So 6291-62-9 is a valid CAS Registry Number.

6291-62-9SDS

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 methyl 3-acetylsulfanylpropanoate

1.2 Other means of identification

Product number -
Other names methyl 3-(acetylsulfanyl)propanoate

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:6291-62-9 SDS

6291-62-9Relevant academic research and scientific papers

Michael addition reaction of thioacetic acid (AcSH) to conjugated alkenes under solvent- and catalyst-free conditions

Sobhani, Sara,Rezazadeh, Soodabeh

experimental part, p. 2076 - 2084 (2010/12/19)

A new and convenient procedure has been developed for the Michael addition reaction of thioacetic acid (AcSH) to a variety of conjugated alkenes under solvent- and catalyst-free conditions. These reactions proceeded in 5-60 min and produced the desired products in good to high yields. Copyright Taylor & Francis Group, LLC.

Novel thiol-derivatized zinc(II) phthalocyanines

García Vior, María C.,Cobice, Diego,Dicelio, Lelia E.,Awruch, Josefina

body text, p. 2467 - 2469 (2009/08/09)

Preparation and characterization of tetrasubstituted zinc(II) phthalocyanines in which sulfur is not linked to the macrocycle are reported herein for the first time. Thioacetic acid S-[3-(3,4-dicyano-phenoxy)-propyl]ester (4) was synthesized in 55% yield

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