631920-67-7 Usage
Description
1-C-[2,4-Bis(1,1-diMethylethoxy)-5-pyriMidinyl]-5-O-(1-Methoxy-1-Methylethyl)-2,3-O-(1-Methylethylidene)-α-D-ribofuranose is a complex organic compound that serves as a crucial intermediate in the synthesis of various biologically significant molecules. Its unique structure, characterized by the presence of multiple functional groups, allows it to participate in a range of chemical reactions, making it a valuable component in the field of biochemistry and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
1-C-[2,4-Bis(1,1-diMethylethoxy)-5-pyriMidinyl]-5-O-(1-Methoxy-1-Methylethyl)-2,3-O-(1-Methylethylidene)-α-D-ribofuranose is used as an intermediate in the synthesis of β-Pseudouridine (O839607) for its role in the development of therapeutic agents. β-Pseudouridine is an isomer of the nucleoside uridine, which is found in all species and in many classes of RNA except mRNA. 1-C-[2,4-Bis(1,1-diMethylethoxy)-5-pyriMidinyl]-5-O-(1-Methoxy-1-Methylethyl)-2,3-O-(1-Methylethylidene)-α-D-ribofuranose is particularly important in the treatment of various diseases and conditions, as it can help regulate cellular processes and maintain overall health.
Used in Biochemical Research:
In the field of biochemical research, 1-C-[2,4-Bis(1,1-diMethylethoxy)-5-pyriMidinyl]-5-O-(1-Methoxy-1-Methylethyl)-2,3-O-(1-Methylethylidene)-α-D-ribofuranose is utilized as a key component in the study of nucleoside metabolism and its role in cellular function. Its involvement in the synthesis of β-Pseudouridine makes it a valuable tool for understanding the mechanisms underlying various biological processes and the development of potential therapeutic strategies.
Used in the Synthesis of Nucleic Acid Analogs:
1-C-[2,4-Bis(1,1-diMethylethoxy)-5-pyriMidinyl]-5-O-(1-Methoxy-1-Methylethyl)-2,3-O-(1-Methylethylidene)-α-D-ribofuranose is also employed in the synthesis of nucleic acid analogs, which are essential for the development of new drugs and therapies targeting genetic disorders and diseases. These analogs can be used to study the structure and function of nucleic acids, as well as to develop novel therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 631920-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,1,9,2 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 631920-67:
(8*6)+(7*3)+(6*1)+(5*9)+(4*2)+(3*0)+(2*6)+(1*7)=147
147 % 10 = 7
So 631920-67-7 is a valid CAS Registry Number.
631920-67-7Relevant articles and documents
A highly stereocontrolled and efficient synthesis of α- and β-pseudouridines
Hanessian, Stephen,Machaalani, Roger
, p. 8321 - 8323 (2003)
A five-step practical and stereocontrolled synthesis of α- and β-pseudouridines from D-ribonolactone is described. The key step involves a highly stereoselective reduction of a hemiketal C-nucleoside intermediate in each case. Multi-gram quantities of β-pseudouridine can now be made available.
