107937-01-9 Usage
Uses
Used in Pharmaceutical Industry:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-8-oxo-3-(1E)-1-propenyl-, (6R,7R)is used as an antimicrobial agent for the treatment of bacterial infections. Its penicillin-like structure and stereochemistry contribute to its effectiveness in combating various types of bacteria.
Used in Research and Development:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-8-oxo-3-(1E)-1-propenyl-, (6R,7R)can be used in research and development for the discovery of new antibiotics and understanding the mechanisms of action of penicillin-like compounds. Its unique structure and stereochemistry make it a valuable tool for studying the interactions between antibiotics and bacterial cells.
Used in Drug Synthesis:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-8-oxo-3-(1E)-1-propenyl-, (6R,7R)can be used as a key intermediate in the synthesis of new antibiotics and related pharmaceutical compounds. Its unique structure and functional groups provide opportunities for further chemical modifications and the development of novel therapeutic agents.
Used in Drug Delivery Systems:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-8-oxo-3-(1E)-1-propenyl-, (6R,7R)can be incorporated into drug delivery systems to improve the efficacy and targeted delivery of antibiotics. Its unique properties may allow for the development of innovative drug delivery platforms, such as nanoparticles or liposomes, to enhance the therapeutic potential of penicillin-like compounds.
Used in Diagnostic Applications:
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-amino-8-oxo-3-(1E)-1-propenyl-, (6R,7R)can be used in diagnostic applications for the detection and identification of bacterial infections. Its unique structure and properties may enable the development of new diagnostic tools, such as biosensors or immunoassays, for the rapid and accurate diagnosis of bacterial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 107937-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,9,3 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107937-01:
(8*1)+(7*0)+(6*7)+(5*9)+(4*3)+(3*7)+(2*0)+(1*1)=129
129 % 10 = 9
So 107937-01-9 is a valid CAS Registry Number.
107937-01-9Relevant academic research and scientific papers
A 7 - amino - 3 - propylene - 1 - yl - 3 - cephem - 4 - carboxylic acid synthesizing method
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Paragraph 0039; 0040; 0044; 0045; 0049; 0050; 0054; 0055, (2017/07/04)
The invention relates to a synthesis method of high-purity 7-amino-3-propylene-1-yl-3-cephem-4-carboxylic acid. The method takes deacetylated-7-aminocephalosporanic acid (D-7-ACA) as a starting raw material, and the starting raw material is reacted with ethyltriphenyl phosphonium bromide through oxidization to generate the 7-amino-3-propylene-1-yl-3-cephem-4-carboxylic acid. The synthesis method has a simple process, low cost and high product yield; the purity is more than 99% and the synthesis method is suitable for industrial production.
PROCESSES FOR THE PREPARATION OF CEPHEM DERIVATIVES
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Page/Page column 18, (2008/06/13)
Provided is a process for preparing a compound of formula 1 or its salt, which includes reacting a compound of formula 2 with a compound of formula 3 in the presence of a base.
PROCESSES FOR THE PREPARATION OF CEPHALOSPORIN DERIVATIVES
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Page/Page column 7-8, (2008/06/13)
Provided is a process for preparing a compound of formula 1 or its salt. The process includes reacting a compound of formula 4 with acetaldehyde in a mixed solvent including water, isopropanol, and methylenechloride in a volume ratio of 1:3-6:11-14 in the
PROCESS FOR THE PREPARATION OF (Z)-ISOMER ENRICHED 7-AMINO-3-PROPEN-1-YL-3-CEPHEM-4- CARBOXYLIC ACID
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Page 12, (2010/02/06)
The invention relates to a process for enrichment of the (Z)-isomer amount in a mixture of the (Z)- and (E)- isomers of 7-amino-3-(1-propen-1-yl)-3-cephem-4-carboxylic acid.
