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2,5-dibromo-1-(4-tolyl)-1H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

366022-82-4

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366022-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 366022-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,6,0,2 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 366022-82:
(8*3)+(7*6)+(6*6)+(5*0)+(4*2)+(3*2)+(2*8)+(1*2)=134
134 % 10 = 4
So 366022-82-4 is a valid CAS Registry Number.

366022-82-4Relevant academic research and scientific papers

A novel and convenient method for the preparation of 5-(diphenylmethylene)-1H-pyrrol-2(5H)-ones; synthesis and mechanistic study

Faigl, Ferenc,Deák, Szilvia,Mucsi, Zoltán,Hergert, Tamás,Balázs, László,Sándor, Boros,Balázs, Barbara,Holczbauer, Tamás,Nyerges, Miklós,Mátrav?lgyi, Béla

, p. 5444 - 5455 (2016)

An efficient, regioselective synthesis has been developed for the preparation of 5-(diphenylmethylene)-1H-pyrrol-2(5H)-ones from readily available 1H-pyrroles by sequential dibromination and selective organometallic bromine/lithium exchange followed by reaction with benzophenone. Comparison of various N-substituents was shown to demonstrate the high tolerance of the transformation to functional groups. The structures of the new products were determined by spectroscopic methods and confirmed by single-crystal X-ray diffraction measurement. In addition, theoretical study of the reaction mechanism and selective functionalization of the endocyclic double bond were also presented.

Influencing the electronic interaction in diferrocenyl-1-phenyl-1H-pyrroles

Hildebrandt, Alexander,Lang, Heinrich

, p. 11831 - 11837 (2011/12/13)

Functionalised diferrocenyl-1-phenyl-1H-pyrroles were synthesised using Negishi C,C cross-coupling reactions. The influence of different substituents at the phenyl moiety on the electronic interaction was studied using electrochemistry (cyclic and square-

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