475469-15-9 Usage
General Description
"(3-Hydroxymethyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester" is a complex synthetic compound that belongs to a class of chemical substances known as esters. (3-HYDROXYMETHYL-PYRROLIDIN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER is characterized by the presence of a carbamic acid unit (which is a derivative of carbamic acid and carries both carboxylic acid and amine substituents) as well as a pyrrolidine ring, a common feature of many natural products, drugs, and experimental substances. The tert-butyl ester component of the molecule refers to the tertiary butyl group attached to the carbamic acid unit, modifying the molecule’s chemical behavior and properties. Due to its complex structure, this chemical is likely used in advanced organic synthesis, potentially serving a crucial role in the pharmaceutical or chemical industries. However, specific applications vary depending on the context of the compound’s synthesis and the overarching goals of the project or research.
Check Digit Verification of cas no
The CAS Registry Mumber 475469-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,4,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 475469-15:
(8*4)+(7*7)+(6*5)+(5*4)+(4*6)+(3*9)+(2*1)+(1*5)=189
189 % 10 = 9
So 475469-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2O3/c1-9(2,3)15-8(14)12-10(7-13)4-5-11-6-10/h11,13H,4-7H2,1-3H3,(H,12,14)
475469-15-9Relevant articles and documents
Synthesis and structure-activity relationships of novel 7-substituted 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic acids as antitumor agents. Part 1
Tomita, Kyoji,Tsuzuki, Yasunori,Shibamori, Koh-ichiro,Tashima, Masanori,Kajikawa, Fumie,Sato, Yuji,Kashimoto, Shigeki,Chiba, Katsumi,Hino, Katsuhiko
, p. 5564 - 5575 (2007/10/03)
In an attempt to search for clinically useful antitumor agents, we have discovered that a series of 1,7-disubstituted-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acids possessed moderate cytotoxic activity. We investigated the structure-acti