88054-42-6 Usage
Description
1-(2-deoxypentofuranosyl)-5-[(4-methylphenyl)sulfanyl]methylpyrimidine-2,4(1H,3H)-dione is a complex chemical compound with a nucleoside structure. It consists of a pyrimidine base and a deoxyribose sugar, which are essential components of DNA. 1-(2-deoxypentofuranosyl)-5-[(4-methylphenyl)sulfanyl]methylpyrimidine-2,4(1H,3H)-dione also contains a sulfur-containing aromatic group, which may confer specific chemical properties to the molecule. The precise function and biological significance of this compound are not readily apparent from its chemical structure, but it likely plays a role in cellular metabolism or nucleic acid biochemistry. Further investigation and experimentation would be necessary to fully understand the properties and potential uses of this compound.
Uses
Since the provided materials do not specify any particular applications for 1-(2-deoxypentofuranosyl)-5-[(4-methylphenyl)sulfanyl]methylpyrimidine-2,4(1H,3H)-dione, we can only speculate on its potential uses based on its chemical structure and components. Some possible applications could include:
Used in Pharmaceutical Industry:
1-(2-deoxypentofuranosyl)-5-[(4-methylphenyl)sulfanyl]methylpyrimidine-2,4(1H,3H)-dione could be used as a potential therapeutic agent for various diseases, particularly those related to nucleic acid metabolism or DNA repair, due to its nucleoside structure and sulfur-containing aromatic group.
Used in Research and Development:
1-(2-deoxypentofuranosyl)-5-[(4-methylphenyl)sulfanyl]methylpyrimidine-2,4(1H,3H)-dione could be utilized in research settings to study the effects of modified nucleosides on cellular processes, such as DNA replication, transcription, and repair. It may also be used to investigate the role of sulfur-containing groups in the chemical properties and interactions of nucleoside analogs.
Used in Chemical Synthesis:
1-(2-deoxypentofuranosyl)-5-[(4-methylphenyl)sulfanyl]methylpyrimidine-2,4(1H,3H)-dione could serve as a starting material or intermediate in the synthesis of more complex molecules with potential applications in various industries, such as pharmaceuticals, materials science, or biotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 88054-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,5 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88054-42:
(7*8)+(6*8)+(5*0)+(4*5)+(3*4)+(2*4)+(1*2)=146
146 % 10 = 6
So 88054-42-6 is a valid CAS Registry Number.
88054-42-6Relevant articles and documents
Conversion of 2'-Deoxyuridine into Thymidine and Related Studies
Reese, Colin B.,Sanghvi, Yogesh S.
, p. 877 - 879 (2007/10/02)
Unprotected 2'-deoxyuridine is converted into thymidine in three steps by a procedure which is equally effective for the 5-methylation of uridine and even more effective for the conversion of 1-β-D-arabinofuranosyluracil into its 5-methyl derivative.