143213-58-5 Usage
Molecular Structure
The compound has a complex molecular structure containing an isoindole-1,3(2H)-dione core and a side chain consisting of 2-(1-methyl-1H-pyrrol-2-yl)-2-oxo-1-phenylethyl.
Core Component
The isoindole-1,3(2H)-dione core is a key structural component of the compound, providing the basis for its chemical properties and potential applications.
Pyrrole Group
The presence of a 1-methyl-1H-pyrrol-2-yl group in the side chain suggests potential pharmaceutical applications, as pyrrole groups are known to exhibit biological activity.
Phenyl Group
The compound also contains a phenyl group, which is another component known for its biological activity and potential pharmaceutical applications.
Biological Activity
The presence of both pyrrole and phenyl groups in the compound indicates that it may have biological activity, making it a candidate for further pharmaceutical research.
Further Studies
To determine the exact properties and potential applications of 1H-Isoindole-1,3(2H)-dione, 2-[2-(1-methyl-1H-pyrrol-2-yl)-2-oxo-1-phenylethyl]-, further studies and research are needed. This may include testing for specific biological activities, assessing pharmacokinetics, and evaluating potential therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 143213-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,1 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143213-58:
(8*1)+(7*4)+(6*3)+(5*2)+(4*1)+(3*3)+(2*5)+(1*8)=95
95 % 10 = 5
So 143213-58-5 is a valid CAS Registry Number.
143213-58-5Relevant articles and documents
Pyrrylphenylethanones related to cathinone and lefetamine: Synthesis and pharmacological activities
Massa,Di Santo,Mai,Artico,Pantaleoni,Giorgi,Coppolino
, p. 403 - 409 (2007/10/02)
The synthesis of various pyrrylphenylethanones resembling cathinone and lefetamine is described starting from 2-chloro-1-(1-methyl-1H-pyrrol-2-yl)2-phenylethan-1-one. Some derivatives showed good antinociceptic activity, comparable to that of morphine. Th
