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(2R,4aR,6R,8aS)-Octahydro-2-<(S)-1-hydroxy-1-methyl-2-<(p-tolylsulfonyl)oxy>ethyl>-6-<(S)-1-(methoxymethoxy)-1,5-dimethylhex-4-enyl>-8a-methylpyrano<3,2-b>pyran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119840-66-3

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119840-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119840-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,4 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119840-66:
(8*1)+(7*1)+(6*9)+(5*8)+(4*4)+(3*0)+(2*6)+(1*6)=143
143 % 10 = 3
So 119840-66-3 is a valid CAS Registry Number.

119840-66-3Upstream product

119840-66-3Relevant academic research and scientific papers

Total Syntheses of (+)-Thyrsiferol, (+)-Thyrsiferyl 23-Acetate, and (+)-Venustatriol

Hashimoto, Masaru,Kan, Toshiyuki,Nozaki, Koji,Yanagiya, Mitsutoshi,Shirahama, Harushia,Matsumoto, Takeshi

, p. 5088 - 5107 (2007/10/02)

The first total syntheses of (+)-thyrsiferol (1), (+)-thyrsiferyl 23-acetate (3), and (+)-venustatriol (5) have been accomplished in a stereoselective manner.An effective synthetic scheme to construct the BC ring system, which adopts a chair/twist-boat conformation, was first developed by means of a model study.This method involves stereoselective formation of the strained C ring by intramolecular attack of the C7-hydroxyl group at the C3-postion of the 2,3-epoxy alcohol, employing titanium tetraisopropoxide as an acidic activator.Based on the information accumulated in the model study and retrosynthetic considerations, the total syntheses of 1,3, and 5 were performed in the sequence of (1) construction of the BC ring system equipped with a C1-C6 carbon unit, (2) elongation of the C17-C24 carbon chain, (3) formation of a D ring through the stereoselective epoxidation of the 4-en-1-ol system and successive cyclization, and (4) construction of the A ring by bromonium ion induced cyclization of the 4-en-1-ol system.

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