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876017-31-1

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876017-31-1 Usage

Molecular structure

1H-Pyrrole-2,5-dione, 3-(2-bromophenyl)-4-(1H-indol-3-yl)-1-methylis a heterocyclic compound derived from pyrrole with a methyl group, a bromophenyl group, and an indolyl group attached to different carbon atoms of the pyrrole ring.

Methyl group

A methyl group (CH3) is attached to the first carbon atom of the pyrrole ring, which may influence the compound's solubility and reactivity.

Bromophenyl group

A bromophenyl group (C6H4Br) is attached to the third carbon atom of the pyrrole ring, which may contribute to the compound's biological activity and lipophilicity.

Indolyl group

An indolyl group (C8H6N) is attached to the fourth carbon atom of the pyrrole ring, which may contribute to the compound's biological activity and potential therapeutic applications.

Pyrrole-2,5-dione core

The compound has a pyrrole-2,5-dione core, which is a key structural feature that may influence its chemical reactivity and potential applications.

Potential biological activity

1H-Pyrrole-2,5-dione, 3-(2-bromophenyl)-4-(1H-indol-3-yl)-1-methylhas potential biological activity, making it a candidate for pharmaceutical research and drug development.

Therapeutic applications

The specific chemical structure and functional groups of this compound make it an interesting target for further investigation and potential therapeutic applications in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 876017-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,0,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 876017-31:
(8*8)+(7*7)+(6*6)+(5*0)+(4*1)+(3*7)+(2*3)+(1*1)=181
181 % 10 = 1
So 876017-31-1 is a valid CAS Registry Number.

876017-31-1Downstream Products

876017-31-1Relevant articles and documents

Synthesis and biological evaluation of novel phenylcarbazoles as potential anticancer agents

Routier, Sylvain,Mérour, Jean-Yves,Dias, Nathalie,Lansiaux, Amélie,Bailly, Christian,Lozach, Olivier,Meijer, Laurent

, p. 789 - 799 (2007/10/03)

We here report the synthesis and biological evaluation of new phenylcarbazole derivatives designed as potential anticancer agents. Indole and hydroxyindole were used to generate three scaffolds that were successively exploited to introduce various substit

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