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508-59-8

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  • Azuleno[4,5-b]furan-2,9-dione,3,3a,4,5,6,6a,9a,9b-octahydro-6a-hydroxy-6,9a-dimethyl-3-methylene-,(3aS,6S,6aS,9aS,9bR)-

    Cas No: 508-59-8

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  • Azuleno[4,5-b]furan-2,9-dione,3,3a,4,5,6,6a,9a,9b-octahydro-6a-hydroxy-6,9a-dimethyl-3-methylene-,(3aS,6S,6aS,9aS,9bR)-

    Cas No: 508-59-8

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508-59-8 Usage

Safety Profile

Poison by intraperitoneal route. Human mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes

Check Digit Verification of cas no

The CAS Registry Mumber 508-59-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 508-59:
(5*5)+(4*0)+(3*8)+(2*5)+(1*9)=68
68 % 10 = 8
So 508-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H18O4/c1-8-4-5-10-9(2)13(17)19-12(10)14(3)11(16)6-7-15(8,14)18/h6-8,10,12,18H,2,4-5H2,1,3H3/t8-,10-,12+,14-,15-/m0/s1

508-59-8SDS

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 Parthenicin

1.2 Other means of identification

Product number -
Other names parthenin

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:508-59-8 SDS

508-59-8Relevant articles and documents

Enantioselective synthesis of neoambrosin, parthenin, and dihydroisoparthenin

Asaoka, Morio,Ohkubo, Taketoshi,Itahana, Hirotsune,Kosaka, Takatoshi,Takei, Hisashi

, p. 3115 - 3128 (2007/10/02)

Enantioselective synthesis of the titled ambrosanolides is described. Use of the trimethylsilyl group as an anchor contributed to the stereoselective introduction of two methyl groups.

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