748812-61-5 Usage
Uses
Used in Pharmaceutical Industry:
(5-BROMO-3-METHYLPYRIDIN-2-YL)CARBAMIC ACID TERT-BUTYL ESTER is used as an intermediate or building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, potentially leading to the discovery of novel therapeutic agents.
Used in Agricultural Industry:
(5-BROMO-3-METHYLPYRIDIN-2-YL)CARBAMIC ACID TERT-BUTYL ESTER is used as a precursor in the synthesis of agrochemicals. Its application in this industry contributes to the development of new pesticides, herbicides, or other agricultural chemicals that can improve crop protection and yield.
Used in Research and Development:
(5-BROMO-3-METHYLPYRIDIN-2-YL)CARBAMIC ACID TERT-BUTYL ESTER is utilized in research and development applications across the pharmaceutical and agricultural industries. Its versatile chemical properties make it a valuable tool for scientists and researchers to explore new chemical reactions, synthesize novel compounds, and investigate potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 748812-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,8,8,1 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 748812-61:
(8*7)+(7*4)+(6*8)+(5*8)+(4*1)+(3*2)+(2*6)+(1*1)=195
195 % 10 = 5
So 748812-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BrN2O2/c1-7-5-8(12)6-13-9(7)14-10(15)16-11(2,3)4/h5-6H,1-4H3,(H,13,14,15)
748812-61-5Relevant academic research and scientific papers
Imidazole acetic acid TAFIa inhibitors: SAR studies centered around the basic P′1 group
Nantermet, Philippe G.,Barrow, James C.,Lindsley, Stacey R.,Young, Marybeth,Mao, Shi-Shan,Carroll, Steven,Bailey, Carolyn,Bosserman, Michele,Colussi, Dennis,McMasters, Daniel R.,Vacca, Joseph P.,Selnick, Harold G.
, p. 2141 - 2145 (2007/10/03)
Structural modifications of the aminopyridine P1 ′ group of imidazole acetic acid based TAFIa inhibitors led to the discovery of the aminocyclopentyl analog 28, a 1nM TAFIa inhibitor with CLT50 functional activity of 14nM but without selectivity against CPB. While not as active, aminobutyl derivative 27 provided an improved 6.7-fold selectivity for TAFIa versus CPB.
