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1-Furan-2-ylmethyl-2,5-diphenyl-1H-pyrrole is a complex organic compound characterized by a unique molecular structure. It features a pyrrole ring, which is a five-membered aromatic ring containing four carbon atoms and one nitrogen atom. The compound is further distinguished by the presence of a 2-furan substituent attached to the methyl group, which is connected to the pyrrole ring. Additionally, two phenyl groups are attached at the 2 and 5 positions of the pyrrole ring, enhancing its stability and reactivity. This chemical is primarily used in the synthesis of various pharmaceuticals and organic compounds due to its diverse functional groups and potential to form multiple bonds. Its chemical formula is C20H15NO, and it has a molecular weight of 283.34 g/mol.

77287-40-2

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77287-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77287-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77287-40:
(7*7)+(6*7)+(5*2)+(4*8)+(3*7)+(2*4)+(1*0)=162
162 % 10 = 2
So 77287-40-2 is a valid CAS Registry Number.

77287-40-2Downstream Products

77287-40-2Relevant academic research and scientific papers

Synthesis of Substituted Pyrroles by Intramolecular Condensation of a Wittig Reagent with the Carbonyl Group of a Tertiary Amide

Cooney, John V.,McEwen, William E.

, p. 2570 - 2573 (1981)

1,2,5-Trisubstituted pyrroles are obtained in 50-100percent yields by addition of the conjugate bases of open-chain analogues of Reissert compounds to the vinyltriphenylphosphonium cation, with subsequent cyclization by an intramolecular Wittig reaction and base-catalyzed elimination of hydrogen cyanide.

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