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Trifluoro-methanesulfonic acid (3S,3aS,4S,6aS,10R,10aR)-4-(tert-butyl-diphenyl-silanyloxymethyl)-3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyloxy)-7,7-dimethyl-1-oxo-3,3a,4,6a,7,8,9,10-octahydro-2-oxa-cyclopenta[d]naphthalen-10-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

329897-85-0

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  • Trifluoro-methanesulfonic acid (3S,3aS,4S,6aS,10R,10aR)-4-(tert-butyl-diphenyl-silanyloxymethyl)-3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyloxy)-7,7-dimethyl-1-oxo-3,3a,4,6a,7,8,9,10-octahydro-2-oxa-cyclopenta[d]naphthalen-10-yl ester

    Cas No: 329897-85-0

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  • Trifluoro-methanesulfonic acid (3S,3aS,4S,6aS,10R,10aR)-4-(tert-butyl-diphenyl-silanyloxymethyl)-3-((1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyloxy)-7,7-dimethyl-1-oxo-3,3a,4,6a,7,8,9,10-octahydro-2-oxa-cyclopenta[d]naphthalen-10-yl ester

    Cas No: 329897-85-0

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  • Shandong Dayi Chemical Co., Ltd.
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329897-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 329897-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,8,9 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 329897-85:
(8*3)+(7*2)+(6*9)+(5*8)+(4*9)+(3*7)+(2*8)+(1*5)=210
210 % 10 = 0
So 329897-85-0 is a valid CAS Registry Number.

329897-85-0Downstream Products

329897-85-0Relevant articles and documents

A short synthesis of Mniopetal F?

Jauch, Johann

, p. 473 - 476 (2007/10/03)

The first total synthesis of Mniopetal F in fourteen steps is reported. Key steps are a new and highly diastereoselective lithium phenylselenide-induced Baylis-Hillman reaction with Feringa's butenolide, an endo-selective intramolecular Diels-Alder reaction (IMDA), inversion of a highly hindered secondary alcohol and a new variant of the Parikh-Doering oxidation.

Synthetic studies towards mniopetals (II). A short synthesis of Mniopetal E

Jauch

, p. 87 - 89 (2007/10/03)

A short total synthesis of Mniopetal E in thirteen steps is reported. Key steps are a new and highly diastereoselective lithium phenylselenide induced Baylis-Hillman reaction with Feringa's butenolide, an endo-selective intramolecular Diels-Alder reaction (IMDA) and a new variant of the Parikh-Doering oxidation.

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