155831-53-1 Usage
Chemical class
Pyrimidine derivatives
Heterocyclic compound
Yes
Composition
Pyrimidine ring with additional functional groups
Functional groups
Ethyl group, phenylselanyl group, benzyloxymethyl group
Presence of heteroatoms
Carbon, Hydrogen, Nitrogen, Oxygen, Selenium
Potential applications
Pharmaceuticals, agrochemicals, materials science
Structure significance
Unique properties due to functional groups
Research and development
Interesting target for further exploration
Molecular weight
Approximately 403.35 g/mol
Appearance
Likely a solid or crystalline compound (based on typical properties of similar compounds)
Solubility
Solvent compatibility not provided, but likely soluble in organic solvents (e.g., methanol, ethanol, acetone) due to the presence of the ethyl and phenyl groups
Stability
Stability information not provided, but generally stable under normal conditions for organic compounds
Reactivity
Reactivity information not provided, but may be influenced by the presence of the phenylselanyl group and the pyrimidine ring
Synthesis
Synthesis method not provided, but likely involves the formation of the pyrimidine ring and subsequent functionalization with the ethyl, phenylselanyl, and benzyloxymethyl groups
Check Digit Verification of cas no
The CAS Registry Mumber 155831-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,3 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155831-53:
(8*1)+(7*5)+(6*5)+(5*8)+(4*3)+(3*1)+(2*5)+(1*3)=141
141 % 10 = 1
So 155831-53-1 is a valid CAS Registry Number.
155831-53-1Relevant articles and documents
A New Route to the Improved Synthesis of 1-(Alkoxymethyl)-5-alkyl- 6-(arylselenenyl)uracils
Lee, Namkyu,Kim, Young-Woo,Kim, Key H.,Kim, Dae-Kee
, p. 659 - 663 (2007/10/03)
A new route to C-6-selenenyl analogs of compound 1a from 5-alkyl-6-chlorouracils 6a-b has been described. A mild and highly efficient synthesis of 1-(alkoxymethyl)-5-alkyl-6-(arylselenenyl)uracils 8a-e has been accomplished from 6a-b in good yields using a two step procedure. Silylation of 5-alkyl-6-chlorouracils 6a-b using N,O-bis(trimethylsilyl)acetamide followed by regioselective alkylation of the silylated intermediate with ethyl or benzyl chloromethyl ether in dichloromethane afforded the desired 1-(alkoxymethyl)-5-alkyl-6-chlorouracils 7a-d in 88-94% yields. Compounds 7a-d readily underwent addition-elimination reaction with an appropriate arylselenol in the presence of ethanolic sodium hyroxide to produce the corresponding 1-(alkoxymethyl)-5-alkyl-6-(arylselenenyl)uracils 8a-e in excellent yields (94-99%).
