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(1R,2S,3R,5R)-2,3-epoxy-5-isopropenyl-2-methylcyclohex-2-enol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128385-82-0

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128385-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128385-82-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128385-82:
(8*1)+(7*2)+(6*8)+(5*3)+(4*8)+(3*5)+(2*8)+(1*2)=150
150 % 10 = 0
So 128385-82-0 is a valid CAS Registry Number.

128385-82-0Downstream Products

128385-82-0Relevant articles and documents

Synthesis of the four epimeric tosylates of (5R)-2,3-epoxy-5-isopropenyl-cyclohexanol

Jones Jr.,Kover

, p. 3907 - 3921 (1995)

Described is the synthesis of the four optically pure epoxytosylates 5, 6, 9 and 12, each with four chiral centers determined, from a single starting material, (R)(-) carvone.

VITAMIN D RECEPTOR ACTIVATORS AND METHODS OF MAKING

-

Page/Page column 28, (2009/05/28)

The invention relates to compounds that are vitamin D receptor activators, compositions comprising such compounds, methods of using such compounds and compositions, processes for preparing such compounds, and intermediates obtained during such processes.

(R)-Carvone as chiral template for the synthesis of some polyols

Brabander, J. De,Kulkarni, B. A.,Garcia-Lopez, R.,Vandewalle, M.

, p. 665 - 670 (2007/10/03)

Some (4S,6R,7R) 4,6,7-trihydroxyheptyl derived building blocks have been obtained from (R)-carvone as the chiral template.A key-step is the Baeyer-Villiger oxidation of a suitable intermediate.

Efficient Enantiospecific Synthesis of Key A-Ring Synthons for the Preparation of 1α,25-Dihydroxyvitamin D3 Using a Chromium((II)-Mediated Reaction

Hatakeyama, Susumi,Numata, Hirotoshi,Osanai, Ken,Takano, Seiichi

, p. 3515 - 3517 (2007/10/02)

Key A-ring synthons for the synthesis of 1α,25-dihydroxyvitamin D3 have been prepared efficiently from (R)-(-)-carvone by use of diastereoselective chromium(II)-mediated addition of an allylic halide to an aldehyde as a key step.

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