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(αR,1R)-ethyl α-hydroxy-2-oxocyclohexaneacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106942-30-7

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106942-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106942-30-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106942-30:
(8*1)+(7*0)+(6*6)+(5*9)+(4*4)+(3*2)+(2*3)+(1*0)=117
117 % 10 = 7
So 106942-30-7 is a valid CAS Registry Number.

106942-30-7Relevant academic research and scientific papers

Chitosan aerogel beads as a heterogeneous organocatalyst for the asymmetric aldol reaction in the presence of water: An assessment of the effect of additives

Gioia, Claudio,Ricci, Alfredo,Bernardi, Luca,Bourahla, Khadidja,Tanchoux, Nathalie,Robitzer, Mike,Quignard, Francoise

, p. 588 - 594 (2013/02/26)

The catalytic properties of chitosan aerogel for the direct asymmetric aldol reaction in water assisted by various surfactants and acid co-catalysts have been evaluated by employing a range of donor and acceptor systems. A beneficial effect on both the yi

Bronsted acid catalyzed asymmetric aldol reaction: A complementary approach to enamine catalysis

Pousse, Guillaume,Cavelier, Fabien Le,Humphreys, Luke,Rouden, Jacques,Blanchet, Jerome

supporting information; experimental part, p. 3582 - 3585 (2010/11/05)

A syn-enantioselective aldol reaction has been developed using Bronsted acid catalysis based on H8-BINOL-derived phosphoric acids. This method affords an efficient synthesis of various β-hydroxy ketones, some of which could not be synthesized u

Organocatalytic enantioselective synthesis of secondary α-hydroxycarboxylates

Dodda, Rajasekhar,Zhao, Cong-Gui

, p. 1605 - 1609 (2008/02/05)

Enantioenriched secondary α-hydroxycarboxylates have been synthesized in good yields and enantioselectivities by using the cross-aldol reaction of ketones and ethyl glyoxylate with a proline-derived dipeptide as the catalyst. Georg Thieme Verlag Stuttgart

A FACILE SYNTHESIS OF (R)-(-)-HEXAHYDROMANDELIC ACID WITH FERMENTING BAKER'S YEAST

Tsuboi, Sadao,Nishiyama, Emiko,Utaka, Masanori,Takeda, Akira

, p. 1915 - 1916 (2007/10/02)

Optically pure (R)-(-)-hexahydromandelic acid has been prepared stereoselectively in two steps by the asymmetric reduction of ethyl α,2-dioxocyclohexaneacetate with fermenting baker's yeast followed by Clemmensen reduction.

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