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(Z)-2-(1,2-diphenylvinyl)-1-methyl-1H-indole-3-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1431973-99-7

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1431973-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431973-99-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,9,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1431973-99:
(9*1)+(8*4)+(7*3)+(6*1)+(5*9)+(4*7)+(3*3)+(2*9)+(1*9)=177
177 % 10 = 7
So 1431973-99-7 is a valid CAS Registry Number.

1431973-99-7Downstream Products

1431973-99-7Relevant academic research and scientific papers

Iron-catalyzed directed C2-alkylation and alkenylation of indole with vinylarenes and alkynes

Wong, Mun Yee,Yamakawa, Takeshi,Yoshikai, Naohiko

, p. 442 - 445 (2015)

An iron-N-heterocyclic carbene catalyst generated from an iron(III) salt, an imidazolinium salt, and a Grignard reagent promotes alkylation and alkenylation reactions at the indole C2-position with vinylarenes and internal alkynes, respectively, via imine-directed C-H activation. The former reaction affords 1,1-diarylalkane derivatives with exclusive regioselectivity. Deuterium-labeling experiments suggest that these reactions involve oxidative addition of the C-H bond to the iron center, insertion of the unsaturated bond into the Fe-H bond, and C-C reductive elimination.

Cobalt-catalyzed ortho-alkenylation of aromatic aldimines via chelation-assisted C-H bond activation

Yamakawa, Takeshi,Yoshikai, Naohiko

, p. 4459 - 4465 (2013/06/26)

An ortho-alkenylation reaction of an aromatic aldimine with an internal alkyne is efficiently promoted by a cobalt catalyst generated from CoBr 2, triarylphosphine, and iPrMgBr. The reaction takes place under mild room-temperature co

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