191354-44-6 Usage
Uses
Used in Laboratory Research:
(S)-3-ACETOXY-4-BROMOBUTYRIC ACID is used as a research compound for [application reason] in laboratory settings. It aids scientists in understanding its chemical properties and potential interactions with other compounds, contributing to the advancement of scientific knowledge.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (S)-3-ACETOXY-4-BROMOBUTYRIC ACID is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a valuable building block, facilitating the development of new drugs with potential therapeutic benefits.
Used in Organic Synthesis:
(S)-3-ACETOXY-4-BROMOBUTYRIC ACID is used as a key component in the synthesis of organic compounds. Its versatility and reactivity make it an essential precursor in the creation of a wide range of chemical products, from specialty chemicals to advanced materials.
Used in Medical Research and Development:
(S)-3-ACETOXY-4-BROMOBUTYRIC ACID is used as a subject of interest in medical research and development. Its potential biological properties are being explored for their possible applications in treating various diseases and conditions, with the aim of discovering new therapeutic agents and improving patient outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 191354-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,3,5 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191354-44:
(8*1)+(7*9)+(6*1)+(5*3)+(4*5)+(3*4)+(2*4)+(1*4)=136
136 % 10 = 6
So 191354-44-6 is a valid CAS Registry Number.
191354-44-6Relevant academic research and scientific papers
Process for preparing(R)-4-cyano-3-hydroxybutyric acid ester
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, (2008/06/13)
The present invention relates to a process for preparing (R)-4-cyano-3-hydroxybutyric acid ester derivatives and more particularly, to a process for preparing optically pure (R)-4-cyano-3-hydroxybutyric acid ester derivatives expressed by formula (1) in high yield by performing cyanation and sequential esterification of (S)-3,4-epoxybutyric acid salt as a starting material. In said formula, R represents linear or branched alkyl group with 1?5 carbon atoms or benzyl group.
