192330-70-4 Usage
General Description
Uridine, 5-chloro-5'-O-[(4-methoxyphenyl)diphenylmethyl]- is a compound that combines uridine, a nucleoside that is an important component of RNA, with a 5-chloro-5'-O-[(4-methoxyphenyl)diphenylmethyl] group. The 5-chloro-5'-O-[(4-methoxyphenyl)diphenylmethyl] group is a halogenated and substituted benzyl group with a methoxyphenyl substituent. Uridine, 5-chloro-5'-O-[(4-methoxyphenyl)diphenylmethyl]- has potential pharmaceutical and research applications due to its unique structure and potential biological activities. It may be used as a research tool in studies related to nucleosides, RNA biology, and medicinal chemistry, and may also have potential therapeutic applications. However, further research is needed to fully understand the properties and potential uses of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 192330-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,3,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 192330-70:
(8*1)+(7*9)+(6*2)+(5*3)+(4*3)+(3*0)+(2*7)+(1*0)=124
124 % 10 = 4
So 192330-70-4 is a valid CAS Registry Number.
192330-70-4Relevant articles and documents
Direct One-Pot Synthesis of Nucleosides from Unprotected or 5-O-Monoprotected d -Ribose
Downey, A. Michael,Richter, Celin,Pohl, Radek,Mahrwald, Rainer,Hocek, Michal
supporting information, p. 4604 - 4607 (2015/09/28)
New, improved methods to access nucleosides are of general interest not only to organic chemists but to the greater scientific community as a whole due their key implications in life and disease. Current synthetic methods involve multistep procedures employing protected sugars in the glycosylation of nucleobases. Using modified Mitsunobu conditions, we report on the first direct glycosylation of purine and pyrimidine nucleobases with unprotected d-ribose to provide β-pyranosyl nucleosides and a one-pot strategy to yield β-furanosides from the heterocycle and 5-O-monoprotected d-ribose.
