136160-42-4 Usage
Pyrimidine derivative
A compound based on the pyrimidine ring structure
Pyrimidine ring
A six-membered heterocyclic ring with four carbon atoms and two nitrogen atoms
Ethyl substituent
A two-carbon alkyl group (-CH2CH3) attached to the 5th position of the pyrimidine ring
Phenylsulfanyl substituent
A phenyl group (-C6H5) with a sulfur atom (-S-) attached to the 6th position of the pyrimidine ring
Cyclohexylmethoxy methyl group
A cyclohexyl group (C6H11) connected to a methoxy group (-OCH3) and a methyl group (-CH3), attached to the nitrogen atom at position 1
Potential pharmaceutical applications
The compound may have uses in the development of drugs due to its diverse biological activities
Biological activities
Antimicrobial, antiviral, and anticancer properties
Further research and testing
Additional studies are required to determine the specific uses and potential benefits of 1-[(cyclohexylmethoxy)methyl]-5-ethyl-6-(phenylsulfanyl)pyrimidine-2,4(1H,3H)-dione
Check Digit Verification of cas no
The CAS Registry Mumber 136160-42-4 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, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136160-42:
(8*1)+(7*3)+(6*6)+(5*1)+(4*6)+(3*0)+(2*4)+(1*2)=104
104 % 10 = 4
So 136160-42-4 is a valid CAS Registry Number.
136160-42-4Relevant 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
