172255-98-0 Usage
Chemical class
Thioxopyrimidines
Explanation
A class of organic compounds characterized by a pyrimidine ring substituted at positions 2 and 4 by sulfur atoms.
Explanation
Thioxopyrimidines, including 1-[(benzyloxy)methyl]-5-(1-methylethyl)-6-(phenylselanyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one, are known to participate in several biological processes, making them of interest for further study.
Explanation
Due to their involvement in biological processes, thioxopyrimidines may have potential applications in the development of new drugs and therapies.
Explanation
The inclusion of a phenylselanyl group in the compound suggests that it may have unique properties and potential applications in organic and medicinal chemistry.
Explanation
The molecular formula represents the total number of each type of atom present in the compound.
Explanation
The molecular weight is a measure of the mass of one mole of the compound, calculated based on the atomic weights of its constituent elements.
Explanation
The compound's structure is defined by the arrangement of its functional groups and the positions they occupy within the molecule.
Explanation
The compound's solubility is not provided, but based on its structure, it may be soluble in organic solvents such as ethanol, methanol, or acetone.
Explanation
The stability of the compound is not provided, but its complex structure suggests that it may be sensitive to certain chemical reactions, such as oxidation or hydrolysis.
Functional groups
Benzyl group, isopropyl group, phenylselanyl group, dihydropyrimidinone ring
Biological processes
Involvement in various biological processes
Pharmacological applications
Potential for use in medicine
Phenylselanyl group
Presence of a phenylselanyl group
Molecular weight
Approximately 490.46 g/mol
Structural features
1-[(benzyloxy)methyl], 5-(1-methylethyl), 6-(phenylselanyl), 2-thioxo-2,3-dihydropyrimidin-4(1H)-one
Solubility
Unknown, but potentially soluble in organic solvents
Stability
Unknown, but may be sensitive to oxidation or hydrolysis
Check Digit Verification of cas no
The CAS Registry Mumber 172255-98-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,2,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 172255-98:
(8*1)+(7*7)+(6*2)+(5*2)+(4*5)+(3*5)+(2*9)+(1*8)=140
140 % 10 = 0
So 172255-98-0 is a valid CAS Registry Number.
172255-98-0Relevant academic research and scientific papers
Pyrimidine acyclonucleoside derivatives
-
, (2008/06/13)
The present invention relates to novel pyrimidine acyclonucleoside derivatives represented by the following general formula (I), antiviral agents containing the derivatives as the active ingredients and processes of preparation thereof. STR1 wherein Rsup
Synthesis and anti-HIV-1 activity of a series of 1-(alkoxymethyl)-5-alkyl-6-(arylselenenyl)uracils and -2-thiouracils
Kim, Dae-Kee,Kim, Young-Woo,Gam, Jongsik,Kim, Ganghyeok,Lim, Jinsoo,Lee, Namkyu,Kim, Hun-Taek,Kim, Key H.
, p. 1275 - 1283 (2007/10/03)
A series of 1-(alkoxymethyl)-5-alkyl-6-(phenylselenenyl)uracils and -2-thiouracils modified at the 3- and/or 5-posiuon of the C-6 phenylselenenyl ring with methyl or fluoro substituent has been synthesized and tested for their ability to inhibit HIV-1 rep
