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(E)-2-(1-phenylprop-1-en-2-yl)-1H-pyrrole is a complex organic compound characterized by a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom. The compound features a phenyl group (C6H5) attached to a prop-1-en-2-yl chain, which is in turn connected to the pyrrole ring. The "E" configuration indicates that the phenyl and vinyl groups are on opposite sides of the double bond in the prop-1-en-2-yl chain. (E)-2-(1-phenylprop-1-en-2-yl)-1H-pyrrole is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also of interest in the field of materials science for its potential use in the development of new polymers and other advanced materials.

2433-76-3

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2433-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2433-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2433-76:
(6*2)+(5*4)+(4*3)+(3*3)+(2*7)+(1*6)=73
73 % 10 = 3
So 2433-76-3 is a valid CAS Registry Number.

2433-76-3Upstream product

2433-76-3Downstream Products

2433-76-3Relevant academic research and scientific papers

Site- and Regioselective Monoalkenylation of Pyrroles with Alkynes via Cp?CoIII Catalysis

Tanaka, Ryo,Ikemoto, Hideya,Kanai, Motomu,Yoshino, Tatsuhiko,Matsunaga, Shigeki

, p. 5732 - 5735 (2016)

A site-, regio-, syn-, and monoselective alkenylation of dimethylcarbamoyl-protected pyrroles proceeded using a catalytic amount of [Cp?Co(CH3CN)3](SbF6)2 and KOAc. A variety of internal alkynes with several fun

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