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The chemical compound "(3aR,4R,6aR,9R,9aS,9bS)-4,9-dihydroxy-9-methyl-3,6-dimethylidenedecahydroazuleno[4,5-b]furan-2(3H)-one" is a complex organic molecule with a unique structure. It features a decalin (a type of cycloalkane) core with a furan ring fused to it, which is a heterocyclic compound containing an oxygen atom in the ring. The molecule has two hydroxyl groups at the 4th and 9th positions, indicating the presence of alcohol functional groups. Additionally, it has a methyl group at the 9th position and a double bond between the 3rd and 6th positions, which is part of the decalin structure. (3aR,4R,6aR,9R,9aS,9bS)-4,9-dihydroxy-9-methyl-3,6-dimethylidenedecahydroazuleno[4,5-b]furan-2(3H)-one is characterized by its specific stereochemistry, with the 'R' and 'S' configurations at various carbon centers, which are crucial for its three-dimensional structure and potential biological activity. The compound's name, derived from the IUPAC nomenclature system, provides a detailed description of its structure, including the positions of functional groups and the stereochemistry of the molecule.

97108-36-6

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97108-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97108-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97108-36:
(7*9)+(6*7)+(5*1)+(4*0)+(3*8)+(2*3)+(1*6)=146
146 % 10 = 6
So 97108-36-6 is a valid CAS Registry Number.

97108-36-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aR,4R,6aR,9R,9aS,9bS)-4,9-dihydroxy-9-methyl-3,6-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one

1.2 Other means of identification

Product number -
Other names Vestenolide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:97108-36-6 SDS

97108-36-6Upstream product

97108-36-6Downstream Products

97108-36-6Relevant academic research and scientific papers

Stereoselective entry to the bicycle [4.3.0] skeleton of oplopanes using a transannular cyclization strategy

Delgado, Guillermo,Guzmán, Salvador

, p. 1006 - 1008 (1999)

Treatment of budlein B with acid gave a H-4β, H-9α- oplopane via lactone cleavage, allylic rearrangement, transannular cyclization and pinacol-type rearrangement. This transformation is stereochemically complementary to that of schkuhfiolide, which produces a H-4α, H-9β- oplopane.

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