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5-(tert-butyldimethylsilyloxy)-3-phenylpentan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

692728-70-4

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692728-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 692728-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,7,2 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 692728-70:
(8*6)+(7*9)+(6*2)+(5*7)+(4*2)+(3*8)+(2*7)+(1*0)=204
204 % 10 = 4
So 692728-70-4 is a valid CAS Registry Number.

692728-70-4Relevant academic research and scientific papers

On the stereoselectivity of alkenoxyl radical 6-exo-trig cyclizations

Schneiders, Nina,Gottwald, Thomas,Hartung, Jens

supporting information; experimental part, p. 797 - 800 (2009/07/05)

The investigated set of 6-exo-trig cyclizations occurs irreversibly and justifies the use of tetrahydropyran-derived transition structures for rationalizing 2,6-cis, 2,5-trans, and 2,4-cis stereoselectivity in ring-closure reactions of 1-, 2-, and 3-pheny

Bromoallenes as allyl dication equivalents in the presence or absence of palladium(0): Direct construction of bicyclic sulfamides containing five- to eight-membered rings by tandem cyclization of bromoallenes

Hamaguchi, Hisao,Kosaka, Shohei,Ohno, Hiroaki,Fujii, Nobutaka,Tanaka, Tetsuaki

, p. 1692 - 1708 (2008/02/03)

A highly regioselective synthesis of bicyclic sulfamides is described. Based on our recent discovery that bromoallenes can act as allyl dication equivalents in the presence of a palladium catalyst and alcohol, we investigated tandem cyclization of bromoal

Stereoselective cyclization using palladium(II) catalyst via hemiacetal intermediates

Miyazawa, Masahiro,Hirose, Yukari,Narantsetseg, Magsarjav,Yokoyama, Hajime,Yamaguchi, Seiji,Hirai, Yoshiro

, p. 2883 - 2886 (2007/10/03)

A stereoselective palladium-catalyzed cyclization of 3-phenyl-7-hydroxy-5- heptenal was developed. The reaction was carried out to give 2,4,6-trisubstituted tetrahydropyran with highly controlled 4,6-cis stereochemistry.

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