136160-32-2 Usage
Chemical structure
A complex structure consisting of a pyrimidine-2,4(1H,3H)-dione core with ethoxymethyl, phenylsulfanyl, and propan-2-yl substituents.
Ethoxymethyl group
An ethyl group attached to a methoxy group.
Phenylsulfanyl group
A phenyl ring bonded to a sulfur atom.
Propan-2-yl group
A branched alkyl group attached to the pyrimidine ring.
Potential applications
May have potential applications in pharmaceuticals, agrochemicals, or materials science.
Unique structure
The combination of the pyrimidine-2,4(1H,3H)-dione core and the substituents gives 1-(ethoxymethyl)-6-(phenylsulfanyl)-5-(propan-2-yl)pyrimidine-2,4(1H,3H)-dione a unique structure.
Biological activity
The compound may have potential biological activity due to its unique structure.
Further research
More research and analysis are needed to fully understand the properties and potential uses of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 136160-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,6 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136160-32:
(8*1)+(7*3)+(6*6)+(5*1)+(4*6)+(3*0)+(2*3)+(1*2)=102
102 % 10 = 2
So 136160-32-2 is a valid CAS Registry Number.
136160-32-2Relevant academic research and scientific papers
Synthesis and Antiviral Activity of Deoxy Analogs of 1--6-(phenylthio)thymine (HEPT) as Potent and Selective Anti-HIV-1 Agents
Tanaka, Hiromichi,Takashima, Hideaki,Ubasawa, Masaru,Sekiya, Kouichi,Nitta, Issei,et al.
, p. 4713 - 4719 (2007/10/02)
The effect of substitution in the acyclic structure of 1--6-(phenylthio)thymine (HEPT) on anti-HIV-1 activity was investigated by synthesizing a series of deoxy analogs and related compounds.Preparation of 1-(2-alkyloxyethoxy)met
