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142705-97-3

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142705-97-3 Usage

Description

(R)-4-Acetylthio-2-pyrrolidinone is a chemical compound derived from pyrrolidinone, a naturally occurring compound, and is characterized by its acetylthio functional group. It is commonly utilized in organic synthesis and pharmaceutical research due to its unique structure and properties, making it a valuable building block for the synthesis of complex molecules. (R)-4-ACETYLTHIO-2-PYRROLIDINONE also holds potential in the development of new drugs, the production of various organic compounds, materials science, and as a reagent in chemical reactions.

Uses

Used in Pharmaceutical Research and Development:
(R)-4-Acetylthio-2-pyrrolidinone is used as a building block for the synthesis of complex molecules in the pharmaceutical industry. Its unique structure and properties contribute to the development of new drugs, making it a crucial component in this field.
Used in Organic Synthesis:
In the field of organic chemistry, (R)-4-Acetylthio-2-pyrrolidinone is used as a versatile compound for the production of various organic compounds. Its acetylthio functional group allows for a wide range of reactions and applications in creating diverse chemical structures.
Used in Materials Science:
(R)-4-Acetylthio-2-pyrrolidinone may also have potential uses in the field of materials science, where its unique properties can be harnessed to develop new materials with specific characteristics.
Used as a Reagent in Chemical Reactions:
Additionally, (R)-4-Acetylthio-2-pyrrolidinone serves as a reagent in various chemical reactions, facilitating the synthesis of different compounds and contributing to the advancement of chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 142705-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,0 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142705-97:
(8*1)+(7*4)+(6*2)+(5*7)+(4*0)+(3*5)+(2*9)+(1*7)=123
123 % 10 = 3
So 142705-97-3 is a valid CAS Registry Number.

142705-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4-ACETYLTHIO-2-PYRROLIDINONE

1.2 Other means of identification

Product number -
Other names Boc-|A-L-dihomo-leucine

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:142705-97-3 SDS

142705-97-3Downstream Products

142705-97-3Relevant articles and documents

Efficient syntheses of (S)-4-hydroxy-2-pyrrolidinone derivatives

Kanno, Osamu,Miyauchi, Masao,Kawamoto, Isao

, p. 173 - 181 (2007/10/03)

Efficient syntheses of (S)-4-hydroxy-2-pyrrolidinone ((5)-2) and (R)4- acetylthio-2-pyrrolidinone (S), which are key intermediates of oral carbapenem CS-834, were studied. The most efficient route to (S)-2 from (S)- 3-hydroxybutyrolactone (8) was accomplished in high yield via (S)-N-allyl-3- (1-ethoxy)ethoxy-4-hydroxybutyramide (14).

Process for preparing optically active 4-mercapto-2-pyrrolidone derivative and intermediate therefor

-

, (2008/06/13)

A process for preparing an optically active 4-mercapto-2-pyrrolidone derivative of the formula [I]: STR1 wherein R1 is a hydrogen atom or a protecting group and R2 is a hydrogen atom or a protecting group, which comprises subjecting

Process for preparing optically active 4-mercapto-2-pyrrolidone derivative and intermediate therefor

-

, (2008/06/13)

A process for preparing an optically active 4-mercapto-2-pyrrolidone derivative of the formula: STR1 wherein a group of the formula: --SR1 is a protected or unprotected mercapto group, and the group of the formula: =NR2 is a protecte

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