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2-(2-bromo-phenyl)-3-oxo-3-phenyl-propionitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

470710-06-6

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470710-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 470710-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,7,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 470710-06:
(8*4)+(7*7)+(6*0)+(5*7)+(4*1)+(3*0)+(2*0)+(1*6)=126
126 % 10 = 6
So 470710-06-6 is a valid CAS Registry Number.

470710-06-6Relevant academic research and scientific papers

Construction of 1,3-Dithio-Substituted Tetralins by [1,5]-Alkylthio Group Transfer Mediated Skeletal Rearrangement

Hisano, Naoya,Kamei, Yuto,Kansaku, Yaoki,Yamanaka, Masahiro,Mori, Keiji

, p. 4223 - 4226 (2018/07/29)

A novel skeletal rearrangement involving a [1,5]-alkylthio group transfer/cyclization sequence is described. Treatment of benzylidene malonates having a thioketal moiety at the homobenzyl position with a catalytic amount of Sc(OTf)3 afforded alkylthio group rearranged adducts in good chemical yields. Detailed investigation of the reaction mechanism revealed that an intramolecular conjugate addition/ring opening sequence (not through-space transfer) is the key to achieving this reaction.

Synthesis of benzo[b]furans via CuI-catalyzed ring closure

Chen, Cheng-Yi,Dormer, Peter G.

, p. 6964 - 6967 (2007/10/03)

A wide variety of benzo[6]furans were synthesized efficiently via a CuI-catalyzed ring closure of 2-haloaromatic ketones. The methodology was tolerant to various functional groups, affording benzofurans in 72-99% yields.

The amine exchange/biaryl coupling sequence: A direct entry to the phenanthro[9,10-d]heterocyclic framework

Olivera, Roberto,SanMartin, Raul,Tellitu, Imanol,Domínguez, Esther

, p. 3021 - 3037 (2007/10/03)

Novel phenanthro[9,10-d]pyrimidines and phenanthro[9,10-d][1,2]oxazoles are regioselectively prepared by the application of a straightforward synthetic pathway, starting from new o,o′-dihalogenated and non-halogenated 4,5-diarylpyrimidines and 4,5-diaryli

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