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(R)-2-cinnamyl-1-tetralone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132797-27-4

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132797-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132797-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,7,9 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132797-27:
(8*1)+(7*3)+(6*2)+(5*7)+(4*9)+(3*7)+(2*2)+(1*7)=144
144 % 10 = 4
So 132797-27-4 is a valid CAS Registry Number.

132797-27-4Downstream Products

132797-27-4Relevant academic research and scientific papers

Stereoselective reactions. 30. Enantioselective alkylation of the lithium enolates of six-membered cyclic ketones using tetradentate chiral amines in the presence of lithium bromide

Murakata, Masatoshi,Yasukata, Tatsuro,Aoki, Takumi,Nakajima, Makoto,Koga, Kenji

, p. 2449 - 2458 (1998)

An efficient enantioselective alkylation of the lithium enolates of cyclohexanone and 1-tetralone with reactive alkyl halides was realized using a stoichiometric amount of a tetradentate chiral amine as a ligand for the lithium in the presence of lithium bromide in toluene.

Stereoselective reactions. Part 31: Catalytic asymmetric alkylation of achiral lithium enolates using a chiral tetradentate amine in the presence of an achiral bidentate amine

Imai, Mitsuko,Hagihara, Atsushi,Kawasaki, Hisashi,Manabe, Kei,Koga, Kenji

, p. 179 - 185 (2007/10/03)

Catalytic asymmetric alkylation of achiral lithium enolates of 1- tetralone and cyclohexanone with reactive alkyl halides was realized by using a combination of a chiral tetradentate amine (~0.05 equiv.) and an achiral bidentate amine (2 equiv.).

Enantioselective Alkylation at the α-Position of Cyclic Ketones using a Chiral Lithium Amide as a Base in the Presence of Lithium Bromide

Murakata, Masatoshi,Nakajima, Makoto,Koga, Kenji

, p. 1657 - 1658 (2007/10/02)

An efficient enantioselective alkylation reaction at the α-position of cyclic ketones (1, 2) can be realized in up to 92percent enantiomeric excess (e.e) by first forming their lithium enolates using a chiral lithium amide 4 in the presence of lithium bromide, followed by treatment with alkyl halides.

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