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(S)-3-(4-fluorophenyl)-3-phenylpropanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863970-22-3

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863970-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863970-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,9,7 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 863970-22:
(8*8)+(7*6)+(6*3)+(5*9)+(4*7)+(3*0)+(2*2)+(1*2)=203
203 % 10 = 3
So 863970-22-3 is a valid CAS Registry Number.

863970-22-3Downstream Products

863970-22-3Relevant academic research and scientific papers

Chiral dihydrobenzo[1,4]oxazines as catalysts for the asymmetric transfer-hydrogenation of α,β-unsaturated aldehydes

Ebner, Christian,Pfaltz, Andreas

, p. 10287 - 10290 (2012/02/01)

A new class of organocatalysts based on the structure of 2,3-dihydrobenzo[1,4]oxazine was prepared and applied in the enantioselective transfer-hydrogenation of α,β-unsaturated aldehydes with Hantzsch ester as hydride donor. These catalysts proved to be particularly effective for the conjugate reduction of β,β-diaryl-substituted acrylaldehydes leading to saturated aldehydes bearing a stereogenic center with two different aryl groups with enantioselectivities of up to 91% ee.

Highly enantioselective 1,4-addition of arylzinc reagents to 3-arylpropenals catalyzed by a rhodium-binap complex in the presence of chlorotrimethylsilane

Tokunaga, Norihito,Hayashi, Tamio

, p. 607 - 613 (2007/10/03)

Asymmetric 1,4-addition of arylzinc chlorides to (E)-3-arylpropenals proceeded with high enantioselectivity in the presence of a rhodium/(R)-binap catalyst and chlorotrimethylsilane to give, after hydrolysis, high yields of the corresponding 3,3-diarylpro

Asymmetric Synthesis of 3,3-Diarylpropanals with Chiral Diene-Rhodium Catalysts

Paquin, Jean-Francois,Defieber, Christian,Stephenson, Corey R. J.,Carreira, Erick M.

, p. 10850 - 10851 (2007/10/03)

A general route to enantioenriched 3,3-diarylpropanals is presented. These useful building blocks are prepared via an asymmetric rhodium-catalyzed conjugate addition of arylboronic acids to cinnamaldehyde derivatives in the presence of chiral dienes. The

Asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated aldehydes catalyzed by a chiral diene-rhodium complex

Hayashi, Tamio,Tokunaga, Norihito,Okamoto, Kazuhiro,Shintani, Ryo

, p. 1480 - 1481 (2007/10/03)

Asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated aldehydes proceeded in the presence of a rhodium catalyst (3 mol %) coordinated with a chiral diene ligand ((R,R)-Bn-bod*) to give the corresponding β-arylaldehydes with perfect 1,4-selectivi

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