943587-40-4 Usage
Uses
Used in Pharmaceutical Industry:
(S)-1-Acetyl-3-pyrrolidinol is used as a chiral building block for the development of various pharmaceuticals, such as antiviral agents, anti-inflammatory drugs, and cardiovascular medications. Its unique stereochemistry allows for the creation of enantiomerically pure compounds, which is crucial for the efficacy and safety of these drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (S)-1-Acetyl-3-pyrrolidinol is utilized in the synthesis of agricultural pesticides and herbicides. Its incorporation into these products contributes to the effectiveness of pest and weed control, supporting agricultural productivity and crop protection.
Overall, (S)-1-Acetyl-3-pyrrolidinol's applications in both the pharmaceutical and agrochemical industries underscore its value as a versatile and essential compound in chemical synthesis and product development.
Check Digit Verification of cas no
The CAS Registry Mumber 943587-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,5,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 943587-40:
(8*9)+(7*4)+(6*3)+(5*5)+(4*8)+(3*7)+(2*4)+(1*0)=204
204 % 10 = 4
So 943587-40-4 is a valid CAS Registry Number.
943587-40-4Relevant academic research and scientific papers
Potassium Thioacids Mediated Selective Amide and Peptide Constructions Enabled by Visible Light Photoredox Catalysis
Liu, Hongxin,Zhao, Liyun,Yuan, Yunfei,Xu, Zhifang,Chen, Kai,Qiu, Shengxiang,Tan, Haibo
, p. 1732 - 1736 (2016/03/15)
A remarkable visible-light-promoted photoredox catalytic methodology involved with amines and eco-friendly potassium thioacids for amide formation was uncovered. This approach can mimic the natural coenzyme acetyl-CoA to selectively acylate amines without affecting other functional groups such as alcohols, phenols, esters, among others. The developed strategy may hold great potential for a comprehensive display of biologically interesting peptide synthesis and amino acid modification through a diacyl disulfide intermediate.
Structure-selectivity relationship in alkyllithium-aldehyde condensations using 3-aminopyrrolidine lithium amides as chiral auxiliaries
Corruble, Aline,Valnot, Jean-Yves,Maddaluno, Jacques,Duhamel, Pierre
, p. 8266 - 8275 (2007/10/03)
A nonracemizing route to a set of chiral 3-aminopyrrolidines, based on 4-hydroxy-(L)-proline, is described. The induction potential of the lithium amides derived from these diamines has then been investigated in the asymmetric addition of alkyllithium com
