474809-21-7 Usage
General Description
"(2-aMino-pyridin-4-ylMethyl)-carbaMic acid tert-butyl ester" is a chemical compound that can be classified under the family of pyridine derivatives. Its structure includes a pyridine ring, often present in many natural products and drug molecules, as well as an amino and carbamic group. The tert-butyl ester group attached to it is often used in organic chemistry as it provides protection for the carbamic acid group during synthesis processes. Its exact properties, such as boiling point, melting point, and solubility, would depend on the precise arrangement of its atoms and specific experimental conditions. Its applications, while not specifically stated, would likely be found in various branches of chemistry, possibly including chemical research and medical drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 474809-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,8,0 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 474809-21:
(8*4)+(7*7)+(6*4)+(5*8)+(4*0)+(3*9)+(2*2)+(1*1)=177
177 % 10 = 7
So 474809-21-7 is a valid CAS Registry Number.
474809-21-7Relevant articles and documents
FACTOR XIIa INHIBITORS
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Paragraph 00254-00255, (2019/11/19)
This invention relates to compounds of formula (I). The compounds of formula (I) are modulators of Factor XII, specifically Factor XIIa. The compounds are inhibitors of Factor XIIa and may be useful as anticoagulants. The compounds of formula (I) may be used in methods of treatment (or prevention) of blood disorders related to bleeding or coagulation.
Absolute stereochemical determination of chiral carboxylic acids
Yang, Qifei,Olmsted, Courtney,Borhan, Babak
, p. 3423 - 3426 (2007/10/03)
(matrix presented) Monoamidation of 1,4-diaminobenzene with α-chiral carboxylic acids leads to a carrier strategy for absolute stereochemical determination with bis-zinc porphyrin tweezers by exciton-coupled circular dichroism (ECCD). The helicity induced in the porphyrin tweezers upon complexation with the derivatized carrier originates from the preferred conformation of the Ccarbonyl-Cchiral bond. Correct ECCD signs can be predicted by the rotamer that places the large group perpendicular to the carbonyl group with the small group facing the porphyrin.
