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(3aS)-3aβ,4,5,5a,6,7,8,9,9a,9bα-Decahydro-9aβ-hydroxy-5aα-methyl-3,9-bis(methylene)naphtho[1,2-b]furan-2(3H)-one is a complex organic compound characterized by a naphtho[1,2-b]furan core with a decalin ring system. It features multiple hydroxyl and methyl groups, as well as a cyclic ketone moiety. The presence of two methylene bridges in the ring system contributes to its unique chemical structure, which may suggest potential pharmacological and biological activities. Further research is required to explore its possible applications.

33530-71-1

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33530-71-1 Usage

Uses

Used in Pharmaceutical Industry:
(3aS)-3aβ,4,5,5a,6,7,8,9,9a,9bα-Decahydro-9aβ-hydroxy-5aα-methyl-3,9-bis(methylene)naphtho[1,2-b]furan-2(3H)-one may be used as a pharmaceutical candidate due to its complex chemical structure and potential biological activities. Its hydroxyl and methyl groups, as well as the cyclic ketone moiety, could allow for interactions with various biological targets, making it a promising compound for the development of new drugs.
Used in Chemical Research:
(3aS)-3aβ,4,5,5a,6,7,8,9,9a,9bα-Decahydro-9aβ-hydroxy-5aα-methyl-3,9-bis(methylene)naphtho[1,2-b]furan-2(3H)-one can also be used in chemical research to study the synthesis and properties of complex organic molecules with fused ring systems. Its unique structure may provide insights into the development of new synthetic methods and the exploration of novel chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 33530-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,3 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33530-71:
(7*3)+(6*3)+(5*5)+(4*3)+(3*0)+(2*7)+(1*1)=91
91 % 10 = 1
So 33530-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-9-5-4-7-14(3)8-6-11-10(2)13(16)18-12(11)15(9,14)17/h11-12,17H,1-2,4-8H2,3H3/t11-,12-,14+,15-/m0/s1

33530-71-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9a-hydroxy-5a-methyl-3,9-dimethylidene-4,5,6,7,8,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one

1.2 Other means of identification

Product number -
Other names Arbusculin C

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33530-71-1 SDS

33530-71-1Downstream Products

33530-71-1Relevant 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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