35565-04-9 Usage
Uses
Used in Pharmaceutical Industry:
(6R)-3-acetoxymethyl-7t-amino-7c-methoxy-8-oxo-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester is used as a pharmaceutical compound for its potential role in the development of new drugs. The presence of various functional groups in its structure may allow for interactions with biological targets, making it a candidate for further research and development in the pharmaceutical field.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6R)-3-acetoxymethyl-7t-amino-7c-methoxy-8-oxo-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester is used as a research compound to study its interactions with biological molecules. Its unique structure and functional groups may provide insights into new mechanisms of action or novel therapeutic approaches.
Used in Organic Synthesis:
(6R)-3-acetoxymethyl-7t-amino-7c-methoxy-8-oxo-(6rH)-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester is used as a synthetic building block in organic synthesis. Its complex structure and functional groups can be utilized to create new molecules with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 35565-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,6 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35565-04:
(7*3)+(6*5)+(5*5)+(4*6)+(3*5)+(2*0)+(1*4)=119
119 % 10 = 9
So 35565-04-9 is a valid CAS Registry Number.
35565-04-9Relevant academic research and scientific papers
HIGHLY STEREOSELECTIVE METHOXYLATION AT THE SEVEN POSITION OF CEPHALOSPORINS
Tsuji, Teruji,Itani, Hikaru,Ishitobi, Hiroyuki
, p. 2745 - 2746 (2007/10/02)
Addition reaction of methanol to 7-methylsulfeniminocephem 1β-oxide derivatives (6 and 12) under acidic conditions gave exclusively 7β-amino-7α-methoxycephem 1β-oxides (7) stabilized by the formation of an intramolecular hydrogen bond between the 7β-amino and the oxygen atom at the 1-position.
