87791-58-0 Usage
Uses
Used in Pharmaceutical Industry:
4-(Benzyloxycarbonyl)-2-azetidinone is used as a building block for the synthesis of various pharmaceuticals, due to its ability to contribute to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 4-(Benzyloxycarbonyl)-2-azetidinone is utilized as a key component in the synthesis of agrochemicals, contributing to the creation of effective pest control agents and other agricultural products.
Used in Organic Synthesis:
4-(Benzyloxycarbonyl)-2-azetidinone is employed as a chiral auxiliary in organic synthesis, facilitating the asymmetric synthesis of a range of organic molecules, which is crucial for the production of enantiomerically pure compounds.
Used in Medicinal Chemistry and Drug Discovery:
4-(Benzyloxycarbonyl)-2-azetidinone is used as a subject of interest in medicinal chemistry and drug discovery, due to its potential biological and pharmacological properties, which may lead to the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 87791-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,9 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87791-58:
(7*8)+(6*7)+(5*7)+(4*9)+(3*1)+(2*5)+(1*8)=190
190 % 10 = 0
So 87791-58-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c13-10-6-9(12-10)11(14)15-7-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,12,13)
87791-58-0Relevant academic research and scientific papers
Ternary nylon-3 copolymers as host-defense peptide mimics: Beyond hydrophobic and cationic subunits
Chakraborty, Saswata,Liu, Runhui,Hayouka, Zvi,Chen, Xinyu,Ehrhardt, Jeffrey,Lu, Qin,Burke, Eileen,Yang, Yiqing,Weisblum, Bernard,Wong, Gerard C. L.,Masters, Kristyn S.,Gellman, Samuel H.
supporting information, p. 14530 - 14535 (2015/01/08)
Host-defense peptides (HDPs) are produced by eukaryotes to defend against bacterial infection, and diverse synthetic polymers have recently been explored as mimics of these natural peptides. HDPs are rich in both hydrophobic and cationic amino acid residu
4-Iodomethylazetidin-2-one
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, (2008/06/13)
Disclosed is a process for preparing 7-(1-hydroxethyl)-3-(2-aminoethylthio)-1-carbadethiaceph-3-em-3-carboxylic acid and its pharmaceutically acceptable salts and esters (I) by total synthesis starting with L-aspartic acid and proceeding via intermediates II and IIa (4-iodomethylazetidin-2-one): STR1
