374796-29-9 Usage
General Description
The chemical 1-Oxa-9-azaspiro[5.5]undecane-9-carboxylic acid, 4-hydroxy-, 1,1-diMethylethyl ester is a compound that belongs to the class of organic compounds known as spiro compounds. It is also known as the 4-hydroxy-1,1-dimethylethyl ester of 1-oxa-9-azaspiro[5.5]undecane-9-carboxylic acid. This chemical may have potential applications in the pharmaceutical industry, as spiro compounds can exhibit various biological activities such as antimicrobial, antiproliferative, and antifungal properties. Further research and study are required to understand the full range of potential uses and implications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 374796-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,4,7,9 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 374796-29:
(8*3)+(7*7)+(6*4)+(5*7)+(4*9)+(3*6)+(2*2)+(1*9)=199
199 % 10 = 9
So 374796-29-9 is a valid CAS Registry Number.
374796-29-9Relevant articles and documents
CYCLOPROPYLAMINE COMPOUND AS LSD1 INHIBITOR AND USE THEREOF
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Paragraph 0179-0180; 0184, (2021/07/24)
Provided is a cyclopropylamine compound as lysine-specific demethylase 1 (LSD1) inhibitor, and a use thereof in preparation of drug for treating diseases associated with LSD1. The cyclopropylamine compound is a compound represented by formula (I), an isomer thereof, and a pharmaceutically acceptable salt thereof.
Spirocyclic amino alcohol building blocks prepared via a Prins-type cyclization in aqueous sulfuric acid
Lukin, Alexey,Bagnyukova, Darya,Kalinchenkova, Natalya,Zhurilo, Nikolay,Krasavin, Mikhail
supporting information, p. 3311 - 3314 (2016/07/11)
A convenient Prins cyclization of various azacycloalkanones with homoallylic alcohol was achieved in aqueous sulfuric acid. The formal four-center, three-component reaction provides a facile and flexible entry into a range of spirocyclic amino alcohols wh