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(5Z)-7-{(1S,4R,5R,6R)-6-[(1E)-3-oxooct-1-en-1-yl]-2,3-dioxabicyclo[2.2.1]hept-5-yl}hept-5-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70711-59-0

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70711-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70711-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,1 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70711-59:
(7*7)+(6*0)+(5*7)+(4*1)+(3*1)+(2*5)+(1*9)=110
110 % 10 = 0
So 70711-59-0 is a valid CAS Registry Number.

70711-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-7-[(1R,4S,5R,6R)-5-[(E)-3-oxooct-1-enyl]-2,3-dioxabicyclo[2.2.1]heptan-6-yl]hept-5-enoic acid

1.2 Other means of identification

Product number -
Other names 15-Ketoprostaglandin G2

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:70711-59-0 SDS

70711-59-0Upstream product

70711-59-0Downstream Products

70711-59-0Relevant academic research and scientific papers

Endoperoxide pathway in prostaglandin biosynthesis in the soft coral Gersemia fruticosa

Varvas, Kuelliki,Koljak, Reet,Jaerving, Ivar,Pehk, Tonis,Samel, Nigulas

, p. 8267 - 8270 (1994)

An acetone powder preparation of the White Sea soft coral Gersemia converts exogenous arachidonic acid to a prostaglandin-endoperoxide, identified as PGG2 by chemical and spectral studies. The latter serves as a key intermediate from which, evidently by nonenzymic transformations, all optically active coral prostaglandins are formed.

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