307531-87-9 Usage
Uses
Used in Pharmaceutical Industry:
[(6-Methyl-3-pyridinyl)(phenylamino)methyl]-, diphenyl ester (9CI) is used as a chemical intermediate for the development of new pharmaceutical compounds. Its unique structural features may contribute to the creation of novel drugs with enhanced biological activity and therapeutic potential.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, [(6-Methyl-3-pyridinyl)(phenylamino)methyl]-, diphenyl ester (9CI) serves as a valuable compound for studying its interactions with various biological targets. Understanding these interactions can lead to the discovery of new drug candidates with improved efficacy and selectivity.
Used in Drug Design and Optimization:
The structural features of [(6-Methyl-3-pyridinyl)(phenylamino)methyl]-, diphenyl ester (9CI) make it a promising candidate for drug design and optimization processes. Its potential use in this application lies in its ability to be modified and combined with other chemical moieties to create more effective and targeted therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 307531-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,5,3 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 307531-87:
(8*3)+(7*0)+(6*7)+(5*5)+(4*3)+(3*1)+(2*8)+(1*7)=129
129 % 10 = 9
So 307531-87-9 is a valid CAS Registry Number.
307531-87-9Relevant academic research and scientific papers
A practical synthesis of a COX-2-specific inhibitor
Davies,Marcoux,Corley,Journet,Cai,Palucki,Wu,Larsen,Rossen,Pye,DiMichele,Dormer,Reider
, p. 8415 - 8420 (2007/10/03)
A number of synthetic strategies to the Cox-2 specific inhibitor 1 have been described. These studies have led to the identification of a novel pyridine construction using annulation of ketone 2 using a vinamidinium species 29 and ammonia in 97% assay yield. Three approaches to the synthesis of ketone 2 are described that allow for its preparation in large quantities in >65% overall yield from methyl 6-methylnicotinate.
