883231-25-2 Usage
General Description
The chemical "[2-[(tert-Butoxycarbonyl)amino]pyrimidin-5-yl]boronic acid" is a boronic acid derivative with a pyrimidine core. It features a boronic acid group attached to a pyrimidine ring, and a tert-butoxycarbonyl (Boc) protecting group attached to the amino group of the pyrimidine. Boronic acids are known for their reactivity in Suzuki coupling reactions, making this compound potentially useful in organic synthesis. The presence of the Boc protecting group also indicates its potential as a building block in organic chemistry, as the Boc group can be removed under mild conditions. [2-[(tert-Butoxycarbonyl)amino]pyrimidin-5-yl]boronic acid may have applications in medicinal chemistry and material science due to the presence of the boronic acid and pyrimidine functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 883231-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,2,3 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 883231-25:
(8*8)+(7*8)+(6*3)+(5*2)+(4*3)+(3*1)+(2*2)+(1*5)=172
172 % 10 = 2
So 883231-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14BN3O4/c1-9(2,3)17-8(14)13-7-11-4-6(5-12-7)10(15)16/h4-5,15-16H,1-3H3,(H,11,12,13,14)
883231-25-2Relevant articles and documents
PROCESS FOR MAKING THIENOPYRIMIDINE COMPOUNDS
-
Page/Page column, (2014/04/18)
Process methods for making the dual mTOR/PI3K inhibitor GDC-0980, named as (S)-1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6-yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one, having the structure: and stereoisomers, geometric isomers, tautomers, and pharmaceutically acceptable salts thereof.
