155831-53-1 Usage
General Description
1-[(benzyloxy)methyl]-5-ethyl-6-(phenylselanyl)pyrimidine-2,4(1H,3H)-dione is a chemical compound belonging to the class of pyrimidine derivatives. It is a heterocyclic organic compound composed of a pyrimidine ring with additional functional groups, including an ethyl group and a phenylselanyl group. The presence of these functional groups gives the compound unique properties and potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science. The compound's structure and properties make it an interesting target for further research and development, as its potential uses and applications continue to be explored.
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%).
