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3-[2]naphthylamino-1-phenyl-propenone is a complex organic compound with the molecular formula C21H17NO. It is characterized by a 3-[2]naphthylamine group attached to a 1-phenyl-propenone moiety. 3-[2]naphthylamino-1-phenyl-propenone is known for its potential applications in the synthesis of various pharmaceuticals and dyes due to its unique chemical structure. The presence of both naphthalene and phenyl rings in the molecule contributes to its stability and reactivity, making it a subject of interest in organic chemistry research. The compound's properties, such as solubility and reactivity, can be influenced by the specific arrangement of its atoms and the presence of functional groups, which can be further explored for its potential uses in chemical and pharmaceutical industries.

4677-11-6

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4677-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4677-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4677-11:
(6*4)+(5*6)+(4*7)+(3*7)+(2*1)+(1*1)=106
106 % 10 = 6
So 4677-11-6 is a valid CAS Registry Number.

4677-11-6Downstream Products

4677-11-6Relevant academic research and scientific papers

Copper-catalyzed carbene insertion and ester migration for the synthesis of polysubstituted pyrroles

Li, Mingrui,Sun, Yiming,Xie, Yuxing,Yu, Yang,Huang, Fei,Huang, He

, p. 11050 - 11053 (2020)

Copper-catalyzed carbene insertion/ester migration/cyclization of enaminones and α-diazo compounds occurred efficiently to afford 2-ester polysubstituted pyrroles under mild conditions in moderate-to-good yields. Substituent functionality was well tolerated and13C-labelled experiments demonstrated 1,2-ester migration during the reaction.

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