117672-15-8 Usage
Chemical structure
A complex structure that includes a five-membered ring and a chain of carbon atoms.
Classification
It is classified as a dienone.
Functional groups
Contains multiple functional groups, including methylthio, trimethoxyphenyl, and pentadienone.
Potential applications
Has potential applications in the pharmaceutical and agricultural industries, as well as in the field of organic synthesis.
Biological activities
May have biological activities and potential therapeutic properties.
Research and development
It is an area of interest for further research and development.
Please note that this list is based on the limited information provided in the material and may not be exhaustive. Further research and analysis would be required to fully understand the properties and potential applications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 117672-15-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,7 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 117672-15:
(8*1)+(7*1)+(6*7)+(5*6)+(4*7)+(3*2)+(2*1)+(1*5)=128
128 % 10 = 8
So 117672-15-8 is a valid CAS Registry Number.
117672-15-8Relevant articles and documents
Convenient one-pot multicomponent strategy for the synthesis of 6-pyrrolylpyrimidines
Dhanalakshmi, Pandi,Shanmugam, Sivakumar
, p. 29493 - 29501 (2014/08/05)
We have developed an easy method to construct diheteroaryls from α-aroylidineketene dithioacetals in a multicomponent manner. The reaction proceeded with high chemo/regioselectivity to yield 4-alkoxy-6-(4-aryl-1H- pyrrol-3-yl)pyrimidin-2-amines under mild
Chemotherapy of leishmaniasis part II: Synthesis and bioevaluation of substituted arylketene dithioacetals as antileishmanial agents
Pandey, Susmita,Suryawanshi,Gupta, Suman,Srivastava
, p. 751 - 756 (2007/10/03)
Some novel aryl substituted ketene dithioacetals 6 (a-d), 9 (a-c) and 10 (a-c) have been synthesized using novel synthetic methods. The compounds were screened against Leishmania donovani in hamsters for their activity profile. Some of the compounds inhibited 50-65% parasite growth at 50mg kg-1 × 5 days.