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The chemical compound "(3aR,4R,5Z,9S,11aS)-9-hydroxy-6-methyl-3,10-dimethylidene-2-oxo-2,3,3a,4,7,8,9,10,11,11a-decahydrocyclodeca[b]furan-4-yl acetate" is a complex organic molecule with a unique structure. It features a decalin ring system with a cyclodeca[b]furan core, which is a type of cyclic ether. The compound has several chiral centers, indicated by the R and S configurations, which determine its stereochemistry. It also contains a hydroxyl group, a carbonyl group, and a methylidene bridge, which contribute to its reactivity and physical properties. The acetate group suggests that it is an ester derivative, which can be hydrolyzed to yield the parent alcohol and acetic acid. (3aR,4R,5Z,9S,11aS)-9-hydroxy-6-methyl-3,10-dimethylidene-2-oxo-2,3,3a,4,7,8,9,10,11,11a-decahydrocyclodeca[b]furan-4-yl acetate is likely to be found in the field of organic chemistry, possibly as an intermediate in the synthesis of more complex molecules or as a component in natural products with potential biological activity.

85847-65-0

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85847-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85847-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,4 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85847-65:
(7*8)+(6*5)+(5*8)+(4*4)+(3*7)+(2*6)+(1*5)=180
180 % 10 = 0
So 85847-65-0 is a valid CAS Registry Number.

85847-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3aR,4R,5Z,9S,11aS)-9-hydroxy-6-methyl-3,10-dimethylidene-2-oxo-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl] acetate

1.2 Other means of identification

Product number -
Other names -

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:85847-65-0 SDS

85847-65-0Upstream product

85847-65-0Downstream Products

85847-65-0Relevant academic research and scientific papers

Biogenetic-type Synthesis of Santonin, Chrysanolide, Dihydrochrysanolide, Tulirinol, Arbusculin-C, Tanacetin, and Artemin

El-Feraly, Farouk S.,Benigni, Daniel A.,McPhail, Andrew T.

, p. 355 - 364 (2007/10/02)

The title compounds were synthsised from their possible biogenetic precursors through hydroperoxide intermediates generated by photo-oxygenation.This route for biological oxygenation may serve as a substitute to epoxidation.The 13C n.m.r. special assignments for all intermediates were made.Single-crystal X-ray analyses unequivocally established the 1S configuration in dihydrochrysanolide (14) and its hydroperoxy-analogue (12).Isomorphous crystals of (12) and (14) belong to the monoclinic system, space group P21, with a = 14.350(6), b = 5.882(3), c = 10.343(3) Angstroem, β = 107.64(2) deg, Z = 2, for (12), and a = 14.461(6), b = 5.887(3), c = 9.698(4) Angstroem, β = 107.44(2) deg, Z = 2, for (14).Least-squares refinement of atomic parameters converged to R 0.040 for (12) and 0.033 for (14) over 1484 and 1300 reflections, respectively, measured by diffractometer.

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