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dimethyl 2-(4-phenylbut-3-en-2-yl)malonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

879480-42-9

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879480-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879480-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,4,8 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 879480-42:
(8*8)+(7*7)+(6*9)+(5*4)+(4*8)+(3*0)+(2*4)+(1*2)=229
229 % 10 = 9
So 879480-42-9 is a valid CAS Registry Number.

879480-42-9Downstream Products

879480-42-9Relevant academic research and scientific papers

Influence of structural changes in ferrocene phosphane aminophosphane ligands on their catalytic activity

?ebesta, Radovan,?kvorcová, Andrea

, p. 1898 - 1902 (2009)

New phosphane aminophosphane ligands based on [3]ferrocenophane skeleton were synthesized using a direct double lithiation followed by phosphanylation. Influence of ligand structure on catalytic performance was evaluated by performing a series of Pd-catalyzed allylic substitution on different substrates. Enantioselectivities up to 55% ee were obtained with bridged ligand compared to 33% ee with analogous non-bridged BoPhoz ligand.

Br?nsted acid and Pd-PHOX dual-catalysed enantioselective addition of activated C-pronucleophiles to internal dienes

Park, Sangjune,Adamson, Nathan J.,Malcolmson, Steven J.

, p. 5176 - 5182 (2019/05/24)

We describe the development of Pd-PHOX-catalysed enantioselective couplings of internal dienes with malononitrile and other activated C-pronucleophiles. Reactions are dramatically accelerated by the addition of Et3N·HBArF4 as a Br?nsted acid co-catalyst, enabling a suite of products bearing a variety of alkyl substituents at the stereogenic carbon to be prepared. A series of mechanism-oriented experiments reveal key aspects of the catalytic cycle and the importance of the non-coordinating BArF4 counterion in not only promoting reactions of internal dienes but also additions of previously unreactive nucleophiles towards terminal dienes.

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