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(3Z,5S)-3-(1-Hydroxyethylidene)-5-[(S)-1-methylpropyl]-2,4-pyrrolidinedione is a chiral chemical compound belonging to the class of pyrrolidinediones and is a derivative of the amino acid proline. It has a molecular formula of C11H17NO3 and is known for its unique structure and potential biological activity. (3Z,5S)-3-(1-Hydroxyethylidene)-5-[(S)-1-methylpropyl]-2,4-pyrrolidinedione's stereochemistry, indicated by the (3Z,5S) designation, highlights its significance in medicinal chemistry and drug development.

75652-74-3

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75652-74-3 Usage

Uses

Used in Organic Synthesis:
(3Z,5S)-3-(1-Hydroxyethylidene)-5-[(S)-1-methylpropyl]-2,4-pyrrolidinedione is used as a key intermediate in organic synthesis for the development of various chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (3Z,5S)-3-(1-Hydroxyethylidene)-5-[(S)-1-methylpropyl]-2,4-pyrrolidinedione is utilized as a starting material or building block for the synthesis of new drugs and medicinal agents. Its unique structure and potential biological activity make it a valuable component in drug discovery and development processes.

Check Digit Verification of cas no

The CAS Registry Mumber 75652-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,5 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75652-74:
(7*7)+(6*5)+(5*6)+(4*5)+(3*2)+(2*7)+(1*4)=153
153 % 10 = 3
So 75652-74-3 is a valid CAS Registry Number.

75652-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5RS)-3-[(Z)-1-hydroxyethylidene]-5-[(S)-1-methylpropyl]-2,4-pyrrolidinedione

1.2 Other means of identification

Product number -
Other names (5RS)-3-((Z)-1-hydroxyethylidene)-5-((S)-1-methylpropyl)-2,4-pyrrolidinedione

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:75652-74-3 SDS

75652-74-3Downstream Products

75652-74-3Relevant academic research and scientific papers

Further Reactions of t-Butyl 3-Oxobutanthioate and t-Butyl 4-Diethylphosphono-3-oxobutanthioate: Carbonyl Coupling Reactions, Amination, Use in The Preparation of 3-Acyltetramic Acids and Application to The Total Synthesis of Fuligorubin A.

Ley, Steven V.,Smith, Stephen C.,Woodward, Peter R.

, p. 1145 - 1174 (2007/10/02)

Key words: Acyltetramic acid; Phosphonate; Wadsworth-Emmons; Dieckmann cyclisation; Fuligorubin A. Abstract: The use of t-butyl-3-oxobutanthioate (1) and t-butyl 4-diethylphosphono-3-oxobuthanthioate (2) for the preparation of homologated derivatives suitable for amination in the presence of silver(I) trifluoroacetate to afford the corresponding β-ketoamides is discussed.In particular Wadsworth-Emmons coupling reactions of (2) with various carbonyl compounds gave good yields of E-substituted products.Many of the β-ketoamides were shown to be suitable precursors for 3-acyltetramic acids using a Dieckman cyclisation with tetra-n-butyl ammonium fluoride as the cyclising base.These new reactions were applied to the total synthesis of the polyene 3-acyltetramic acid fuligorubin A.

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