852633-82-0 Usage
Uses
Used in Pharmaceutical Industry:
4-Morpholinophenylglyoxal hydrate is used as a key intermediate in the synthesis of various organic molecules for the development of new drugs. Its unique structure allows for the creation of compounds with potential antitumor, antibacterial, and antifungal properties, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Morpholinophenylglyoxal hydrate is utilized as a precursor in the production of effective pesticides and other crop protection agents. Its ability to form a wide range of organic molecules makes it a valuable component in the synthesis of compounds with pesticidal and fungicidal activities, enhancing crop yield and quality.
Overall, 4-Morpholinophenylglyoxal hydrate plays a significant role in both the pharmaceutical and agrochemical industries, driving innovation and the development of novel compounds with therapeutic and protective properties.
Check Digit Verification of cas no
The CAS Registry Mumber 852633-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,6,3 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 852633-82:
(8*8)+(7*5)+(6*2)+(5*6)+(4*3)+(3*3)+(2*8)+(1*2)=180
180 % 10 = 0
So 852633-82-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO3.H2O/c14-9-12(15)10-1-3-11(4-2-10)13-5-7-16-8-6-13;/h1-4,9H,5-8H2;1H2
852633-82-0Relevant articles and documents
Metal-free dual sp3 C-H functionalization: I2- promoted domino oxidative cyclization to construct 2,5-disubstituted oxazoles
Gao, Qing-He,Fei, Zhuan,Zhu, Yan-Ping,Lian, Mi,Jia, Feng-Cheng,Liu, Mei-Cai,She, Neng-Fang,Wu, An-Xin
, p. 22 - 28 (2013/01/15)
An I2-promoted sp3 C-H functionalization has been developed for the synthesis of 2,5-disubstituted oxazoles from easily available methyl ketones and benzylamines without any metal and peroxide catalyst. This domino oxidative cyclization process involves the cleavage of C-H bond and the formation of C-N, C-O bonds.
