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Azuleno[4,5-b]furan-2(3H)-one, decahydro-3,4-dihydroxy-3-(2-hydroxypropyl)-6,9-bis(methylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106533-22-6

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106533-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106533-22-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106533-22:
(8*1)+(7*0)+(6*6)+(5*5)+(4*3)+(3*3)+(2*2)+(1*2)=96
96 % 10 = 6
So 106533-22-6 is a valid CAS Registry Number.

106533-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8α,11α-dihydroxy-13-(1'-hydroxyethyl)-11-epicostus lactone

1.2 Other means of identification

Product number -
Other names (3S,3aR,4S,6aR,9aR,9bR)-3,4-Dihydroxy-3-(2-hydroxy-propyl)-6,9-dimethylene-decahydro-azuleno[4,5-b]furan-2-one

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:106533-22-6 SDS

106533-22-6Downstream Products

106533-22-6Relevant academic research and scientific papers

Chemical Transformation of Deacylsubexpinnatin into the Natural Oxetane Lactone Subexpinnatin C

Collado, Isidro G.,Macias, Francisco A.,Massanet, Guillermo M.,Molinillo, Jose Maria G.,Luis, Francisco R.

, p. 3323 - 3326 (1987)

Subexpinnatin C (5), a secondary metabolite isolated from Centaurea canariensis Brouss. (var. subexpinnata Burch.), has been regio- and stereoselectively synthesized from deacylsubexpinnatin (11).This transformation involves a photoaddition reaction and a new method of obtaining the oxetane ring.

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