125056-94-2 Usage
Chemical class
Pyrimidine derivatives
Pyrimidine ring
Contains two oxygen atoms
Hydroxyethoxy methyl group
Suggests potential solubility in water
Phenylsulfanyl group
May confer specific chemical properties and potential reactivity
Prop-1-yn-1-yl group
May confer specific chemical properties and potential reactivity
Potential applications
Pharmaceutical intermediate, chemical reagent, synthesis of other compounds
Further research needed
To fully understand its properties and potential uses
Please note that this is a complex chemical compound, and further research and study would be needed to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 125056-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,5 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125056-94:
(8*1)+(7*2)+(6*5)+(5*0)+(4*5)+(3*6)+(2*9)+(1*4)=112
112 % 10 = 2
So 125056-94-2 is a valid CAS Registry Number.
125056-94-2Relevant academic research and scientific papers
6-substituted acyclopyrimidine nucleoside derivatives and antiviral agents containing the same as active ingredient thereof
-
, (2008/06/13)
6-substitutted acyclopyrimidine nucleoside derivatives represented by the following general formula I: STR1 wherein R1 represents a hydrogen or halogen atom or a group of alkyl, alkenyl, alkynyl, alkylcarbonyl, arylcarbonyl, arylcarbonylalkyl,
A new class of HIV-1-specific 6-substituted acyclouridine derivatives: Synthesis and anti-HIV-1 activity of 5- or 6-substituted analogues of 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)
Tanaka,Baba,Hayakawa,Sakamaki,Miyasaka,Ubasawa,Takashima,Sekiya,Nitta,Shigeta,Walker,Balzarini,De Clercq
, p. 349 - 357 (2007/10/02)
A series of novel acyclouridine derivatives substituted at both the C-5 and C-6 positions were synthesized for the purpose of improving the activity of a recently reported HIV-1-specific lead, 1-[(2-hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT). Prep
