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Propanoic acid, 2-[(3-methoxy-3-oxopropyl)thio]-, ethyl ester is a chemical compound characterized by the molecular formula C9H16O4S. It is an ethyl ester derivative of propanoic acid, featuring a thioester functional group. Propanoic acid, 2-[(3-methoxy-3-oxopropyl)thio]-, ethyl ester is known for its reactivity due to the presence of the thioester group, which enables it to engage in a range of chemical reactions. It serves as a crucial intermediate in the synthesis of various compounds across different industries, including pharmaceuticals and agrochemicals, and also finds application as a flavoring agent in the food industry.

66319-05-9

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66319-05-9 Usage

Uses

Used in Pharmaceutical Industry:
Propanoic acid, 2-[(3-methoxy-3-oxopropyl)thio]-, ethyl ester is utilized as a key intermediate in the synthesis of pharmaceutical compounds. Its reactivity and functional group make it suitable for the development of new drugs and medicinal agents.
Used in Agrochemical Industry:
In the agrochemical sector, Propanoic acid, 2-[(3-methoxy-3-oxopropyl)thio]-, ethyl ester is employed as an intermediate for the production of various agrochemicals. Its role in the synthesis process is vital for creating effective and targeted agrochemical products.
Used in Food Industry:
Propanoic acid, 2-[(3-methoxy-3-oxopropyl)thio]-, ethyl ester is used as a flavoring agent, contributing to the taste and aroma profiles of various food products. Its ability to impart specific flavors makes it a valuable component in the creation of food additives and flavorings.
Overall, Propanoic acid, 2-[(3-methoxy-3-oxopropyl)thio]-, ethyl ester is a versatile chemical intermediate with applications in multiple industries, primarily due to its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 66319-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,1 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66319-05:
(7*6)+(6*6)+(5*3)+(4*1)+(3*9)+(2*0)+(1*5)=129
129 % 10 = 9
So 66319-05-9 is a valid CAS Registry Number.

66319-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(3-methoxy-3-oxopropyl)sulfanylpropanoate

1.2 Other means of identification

Product number -
Other names Propanoic acid,2-[(3-methoxy-3-oxopropyl)thio]-,ethyl 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:66319-05-9 SDS

66319-05-9Relevant academic research and scientific papers

MORPHOLINO SUBSTITUTED BICYCLIC PYRIMIDINE UREA OR CARBAMATE DERIVATIVES AS MTOR INHIBITORS

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Page/Page column 45; 70, (2013/04/24)

The invention relates to compounds of formula (I) wherein m, o, Ra, Rb, R1 and T1 have the meaning as cited in the description and the claims. Said compounds are useful as inhibitors of mTOR for the treatment or prophylaxis of mTOR related diseases and disorders. The invention also relates to pharmaceutical compositions including said compounds, the preparation of such compounds as well as the use as medicaments

Stereoisomeric Flavor Substances XXXI. - Tetrahydro-2-methylthiophen-3-ol - Structure and Properties of the Stereoisomers

Mosandl, Armin,Hener, Uwe,Fenske, Heinz-Dieter

, p. 859 - 862 (2007/10/02)

Tetrahydro-2-methylthiophen-3-ol (6) has been synthesized and separated by liquid chromatography to yield cis(6a/6a') and trans isomers (6b/6b').Using (S)-tetrahydro-5-oxo-2-furancarboxylic acid chloride, 6a/6a' and 6b/6b' are transformed into the diastereomeric esters 7 - 10 which are separated by liquid chromatography.Hydrolysis of the esters yields the optically pure stereoisomers 6a, 6a', 6b, and 6b'.Absolute configuration and sensory characteristics of these stereoisomers are given.

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