655233-39-9 Usage
Uses
Used in Pharmaceutical Industry:
(6R,7R)-7-AMINO-8-OXO-3-((2S)-TETRAHYDROFURAN-2-YL)-5-THIA-1-AZABICYCLO[4.2.0]OCT-2-ENE-2-CARBOXYLIC ACID 4-NITROBENZYL ESTER HCL is used as a pharmaceutical compound for its potential therapeutic applications. (6R,7R)-7-AMINO-8-OXO-3-((2S)-TETRAHYDROFURAN-2-YL)-5-THIA-1-AZABICYCLO[4.2.0]OCT-2-ENE-2-CARBOXYLIC ACID 4-NITROBENZYL ESTER HCL's unique structure and chemical properties allow it to interact with biological targets, making it a candidate for the development of new drugs to treat various diseases.
Used in Drug Synthesis:
In the field of drug synthesis, (6R,7R)-7-AMINO-8-OXO-3-((2S)-TETRAHYDROFURAN-2-YL)-5-THIA-1-AZABICYCLO[4.2.0]OCT-2-ENE-2-CARBOXYLIC ACID 4-NITROBENZYL ESTER HCL serves as a key intermediate or building block in the synthesis of more complex pharmaceutical agents. Its versatile functional groups enable further chemical modifications to optimize the drug's efficacy, selectivity, and pharmacokinetic properties.
Used in Medicinal Chemistry Research:
(6R,7R)-7-AMINO-8-OXO-3-((2S)-TETRAHYDROFURAN-2-YL)-5-THIA-1-AZABICYCLO[4.2.0]OCT-2-ENE-2-CARBOXYLIC ACID 4-NITROBENZYL ESTER HCL is utilized in medicinal chemistry research to explore its binding affinity, selectivity, and mechanism of action against various biological targets. Understanding the compound's interactions with these targets can provide valuable insights into the design of more effective and selective drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 655233-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,5,2,3 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 655233-39:
(8*6)+(7*5)+(6*5)+(5*2)+(4*3)+(3*3)+(2*3)+(1*9)=159
159 % 10 = 9
So 655233-39-9 is a valid CAS Registry Number.
655233-39-9Relevant articles and documents
Development of an alternative process for the manufacture of a key starting material for cefovecin sodium
Norris, Timothy,Nagakura, Isao,Morita, Hiromasa,McLachlan, Grant,Desneves, Joe
, p. 742 - 746 (2012/12/29)
A process has been developed for the use of trimethylphosphite for the formation of the six-membered 3,6-dihydro-2H-[1,3]-thiazine ring in the cephem architecture by an intramolecular Horner-Emmons-Wadsworth condensation. The process is a suitable alternative to the traditional Wittig process, which uses trimethylphosphine. The process developed is a highly telescoped reaction pathway consisting of at least six known reaction intermediates that was scaled for production use to produce 2.
PROCESS FOR PREPARING CEPHALOSPORIN INTERMEDIATES USING α-IODO-1-AZETIDINEACETIC ACID ESTERS AND TRIALKYLPHOSPHITES
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Page/Page column 17-18, (2010/02/14)
This invention relates a process for preparing a compound of formula (I), wherein R1 is para-nitrobenzyl or allyl; X is halo; as well as its isomers.