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5-(4-methyl-5-phenylfuran-2-yl)benzo[d][1,3]dioxole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1443441-66-4

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1443441-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1443441-66-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,4,4 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1443441-66:
(9*1)+(8*4)+(7*4)+(6*3)+(5*4)+(4*4)+(3*1)+(2*6)+(1*6)=144
144 % 10 = 4
So 1443441-66-4 is a valid CAS Registry Number.

1443441-66-4Downstream Products

1443441-66-4Relevant academic research and scientific papers

Domino Radical Addition/Oxidation Sequence with Photocatalysis: One-Pot Synthesis of Polysubstituted Furans from α-Chloro-Alkyl Ketones and Styrenes

Wang, Shuang,Jia, Wen-Liang,Wang, Lin,Liu, Qiang,Wu, Li-Zhu

supporting information, p. 13794 - 13798 (2016/09/21)

A new domino reaction has been developed that allows the combination of styrenes and α-alkyl ketone radicals to afford a wide array of polysubstituted furans in good to excellent yields under mild and simple reaction conditions. The key to success of this novel protocol is the use of photocatalyst fac-Ir(ppy)3and oxidant K2S2O8. Mechanistic studies by a radical scavenger and photoluminescence quenching suggest that a radical addition/oxidation pathway is operable.

Regioselective Synthesis of Multisubstituted Furans via Copper-Mediated Coupling between Ketones and β-Nitrostyrenes

Ghosh, Monoranjan,Mishra, Subhajit,Hajra, Alakananda

, p. 5364 - 5368 (2015/05/27)

A copper-mediated intermolecular annulation of alkyl ketones and β-nitrostyrenes has been developed for the regioselective synthesis of multisubstituted furan derivatives in good yields. This protocol is applicable to both cyclic and acyclic ketones. (Che

Copper-catalyzed regioselective synthesis of furan via tandem cycloaddition of ketone with an unsaturated carboxylic acid under air

Ghosh, Monoranjan,Mishra, Subhajit,Monir, Kamarul,Hajra, Alakananda

, p. 309 - 314 (2015/01/16)

A catalytic decarboxylative annulation has been developed for the regioselective synthesis of trisubstituted furans by the cycloaddition of ketones with α,β-unsaturated carboxylic acids under ambient air. A library of furan derivatives were obtained in good yields from the readily available substrates in the combination of a catalytic amount of Cu-salt and a stoichiometric amount of water. Water plays a crucial role in this catalytic transformation. This journal is

Synthesis of polysubstituted furans via copper-mediated annulation of alkyl ketones with α,β-unsaturated carboxylic acids

Yang, Yuzhu,Yao, Jinzhong,Zhang, Yuhong

supporting information, p. 3206 - 3209 (2013/07/26)

A novel copper-mediated annulation of alkyl ketones with α,β-unsaturated carboxylic acids has been accomplished. This reaction provides a facile and regio-defined method for the synthesis of 2,3,5-trisubstituted furans from simple chemical reagents.

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