10390-44-0 Usage
Uses
Used in Pharmaceutical Industry:
(6R,7R)-3-[(Acetyloxy)methyl]-8-oxo-7-[(phenoxyacetyl)amino]-5-thia-1-azabicyclo[4.2.0]octane-2-ene-2-carboxylic acid is used as a potential therapeutic agent for various medical conditions due to its complex structure and functional groups that may be involved in acetylation, amidation, and redox reactions.
Used in Drug Metabolism and Synthesis:
In the pharmaceutical industry, this compound is used as a key intermediate in the synthesis of other drugs, taking advantage of its ability to participate in acetylation and amidation reactions, which are essential in drug metabolism and synthesis.
Used in Drug Delivery Systems:
(6R,7R)-3-[(Acetyloxy)methyl]-8-oxo-7-[(phenoxyacetyl)amino]-5-thia-1-azabicyclo[4.2.0]octane-2-ene-2-carboxylic acid can be employed in the development of novel drug delivery systems to improve the bioavailability and therapeutic outcomes of various medications by enhancing their delivery and targeting specific biological targets.
Used in Research and Development:
(6R,7R)-3-[(Acetyloxy)methyl]-8-oxo-7-[(phenoxyacetyl)amino]-5-thia-1-azabicyclo[4.2.0]octane-2-ene-2-carboxylic acid is also used in research and development for studying its potential interactions with biological targets and exploring its therapeutic properties, which could lead to the discovery of new drugs or治疗方法 (治疗方法, which means "treatment methods" in Chinese) for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 10390-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10390-44:
(7*1)+(6*0)+(5*3)+(4*9)+(3*0)+(2*4)+(1*4)=70
70 % 10 = 0
So 10390-44-0 is a valid CAS Registry Number.
10390-44-0Relevant articles and documents
Optically-detectable enzyme substrates and their method of use
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, (2008/06/13)
The present invention relates to compounds that are substrates for an enzyme, and upon reaction with the enzyme provide a detectable response, such as an optically detectable response. In particular, the compounds have utility in detecting the presence of
Selective conversion of benzyl alcohol carboxylates to the free acid form
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, (2008/06/13)
A process for preparing free carboxylic acids which comprises treating an optionally substituted benzyl ester with a Lewis acid, preferably in the presence of a cation acceptor, followed by hydrolysis, if required.