144478-37-5 Usage
Molecular structure
1H-Indole, 1-[(4-methylphenyl)sulfonyl]-5-(methylsulfinyl)has a complex molecular structure with an indole core, sulfonyl group, and methylsulfinyl group attached to it.
Class of compounds
It belongs to the class of indole compounds, which are commonly found in plants and known for their pharmacological and biological activities.
Sulfonyl group
The presence of a sulfonyl group (-SO2-) in the compound, which is an important functional group in organic chemistry, known for its reactivity and diverse properties.
Methylsulfinyl group
The presence of a methylsulfinyl group (-SO(CH3)-) in the compound, another important functional group in organic chemistry, known for its reactivity and diverse properties.
Potential applications
Due to the presence of sulfonyl and methylsulfinyl groups, this compound may have potential applications in pharmaceuticals or agrochemicals, as these functional groups are often associated with diverse properties and reactivities.
Further research needed
More research is required to fully understand the potential uses and properties of 1H-Indole, 1-[(4-methylphenyl)sulfonyl]-5-(methylsulfinyl)-, as its complex molecular structure and functional groups may lead to a variety of possible applications and interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 144478-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,7 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 144478-37:
(8*1)+(7*4)+(6*4)+(5*4)+(4*7)+(3*8)+(2*3)+(1*7)=145
145 % 10 = 5
So 144478-37-5 is a valid CAS Registry Number.
144478-37-5Relevant articles and documents
SYNTHESIS OF SOME 5-SUBSTITUTED INDOLES
Yang, Youhua,Martin, Arnold R.,Nelson, David L.,Regan, John
, p. 1169 - 1175 (2007/10/02)
A halogen-metal exchange strategy was employed to prepare several 5-substituted indoles from 5-bromoindole.Additional derivatives were elaborated from the formyl, acetyl, thiomethyl, boronic acid and trimethylstannyl analogues thus prepared.
