91255-08-2 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
Pyrido[4,3-d]pyrimidin-4(3H)-one, 5-amino-3-(phenylmethyl)is utilized as a key intermediate in the synthesis of new drugs targeting a range of biological pathways and receptors. Its unique structure allows for the exploration of structure-activity relationships and potential drug interactions, contributing to the advancement of medicinal chemistry.
Used in the Synthesis of Novel Drugs:
In the pharmaceutical industry, Pyrido[4,3-d]pyrimidin-4(3H)-one, 5-amino-3-(phenylmethyl)is employed as a building block for the development of innovative therapeutic agents. Its potential biological activity and versatile chemical properties make it suitable for the creation of drugs with improved efficacy and selectivity.
Used in Structure-Activity Relationship Studies:
Pyrido[4,3-d]pyrimidin-4(3H)-one, 5-amino-3-(phenylmethyl)serves as an important molecule in the investigation of structure-activity relationships. By studying its interactions with various biological targets, researchers can gain insights into the design of more effective and safer drugs.
Further research is necessary to fully understand the potential uses and therapeutic benefits of Pyrido[4,3-d]pyrimidin-4(3H)-one, 5-amino-3-(phenylmethyl)-, as its unique structure and potential biological activity hold promise for the development of novel pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 91255-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,5 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91255-08:
(7*9)+(6*1)+(5*2)+(4*5)+(3*5)+(2*0)+(1*8)=122
122 % 10 = 2
So 91255-08-2 is a valid CAS Registry Number.
91255-08-2Relevant academic research and scientific papers
Granik, V. G.,Grizik, S. I.,Kiselev, S. S.,Chistyakov, V. V.,Anisimova, O. S.,Solov'eva, N. P.
, p. 434 - 439 (1984)
The reaction of 1-benzyl-5-cyano-6-dimethylaminomethylene-1,6-dihydro-4-pyrimidinone with acid leads to 5-benzyl-1,2,7,8-tetrahydropyridopyrimidine-1,8-dione, whereas the reaction with ammonia leads to a mixture of 3-cyano-4-benzylamino-2-pyridone
