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ethyl 7-chloro-2-phenyl-1H-indole-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1440422-69-4

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1440422-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440422-69-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,0,4,2 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1440422-69:
(9*1)+(8*4)+(7*4)+(6*0)+(5*4)+(4*2)+(3*2)+(2*6)+(1*9)=124
124 % 10 = 4
So 1440422-69-4 is a valid CAS Registry Number.

1440422-69-4Downstream Products

1440422-69-4Relevant articles and documents

Copper-Mediated One-Pot Synthesis of Indoles through Sequential Hydroamination and Cross-Dehydrogenative Coupling Reaction

Cai, Yichao,Chen, Chunxia,Chen, Xin,Liu, Yajie,Peng, Jinsong,Song, Zirui,Sun, Peng,Yang, Jiaojiao

, p. 75 - 84 (2020)

Starting from simple anilines and ester arylpropiolates, an efficient one-pot synthesis of 2-arylindole-3-carboxylate derivatives has been developed through copper-mediated sequential hydroamination and cross-dehydrogenative coupling (CDC) reaction. The i

Copper-Catalyzed Synthesis of Multisubstituted Indoles through Tandem Ullmann-Type C-N Formation and Cross-dehydrogenative Coupling Reactions

Li, Yue,Peng, Jinsong,Chen, Xin,Mo, Baichuan,Li, Xue,Sun, Peng,Chen, Chunxia

, p. 5288 - 5294 (2018/05/17)

Multisubstituted indoles were synthesized via a one-pot tandem copper-catalyzed Ullmann-type C-N bond formation/intramolecular cross-dehydrogenative coupling process at 130 °C in DMSO. The methodology allows practical and modular assembly of indoles in go

Iodide-Ion-Catalyzed carbon-carbon bond-forming cross-dehydrogenative coupling for the synthesis of indole derivatives

Jia, Zhenhua,Nagano, Takashi,Li, Xingshu,Chan, Albert S. C.

supporting information, p. 858 - 861 (2013/03/14)

The nBu4NI-catalyzed intramolecular cross-dehydrogenative coupling (CDC) reaction has been applied to the synthesis of 1H-indole derivatives. Intramolecular oxidative coupling of N-arylenamines proceeded in the presence of a catalytic amount of nBu4NI and tert-butyl hydroperoxide (TBHP) to afford the corresponding 1H-indole derivatives in good-to-excellent yields. A preliminary study of the synthesis of 3H-indole is also reported. This is a rare example of the nBu4NI-catalyzed C-C bond-forming CDC reaction. Copyright

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