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4-Octene-1,8-diol, diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76293-63-5

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76293-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76293-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,2,9 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76293-63:
(7*7)+(6*6)+(5*2)+(4*9)+(3*3)+(2*6)+(1*3)=155
155 % 10 = 5
So 76293-63-5 is a valid CAS Registry Number.

76293-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,8-diacetoxy-4-octene

1.2 Other means of identification

Product number -
Other names diacetoxy-1,8 octene-4

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:76293-63-5 SDS

76293-63-5Downstream Products

76293-63-5Relevant academic research and scientific papers

METATHESE D'ACETATES D'ALCOOLS ω-INSATURES. SYNTHESE DE PHEROMONES D'INSECTES

Levisalles, Jaques,Villemin, Didier

, p. 3181 - 3186 (2007/10/02)

Esters of alkenoic acids, including insect pheromones as examples, have been synthesized using alkene metathesis reactions.

SYNTHESE DE MACROLIDES PAR METATHESE.

Villemin, Didier

, p. 1715 - 1718 (2007/10/02)

Two syntheses of macrolides via olefin metathesis are presented.The first (A) involves preparation of ω-hydroxyacid 6 or 9 by metathesis followed by cyclisation, while the second (B) involves macrocyclic ring closure by metathesis of a ω,ω'diunsaturated ester 12.

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