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5811-94-9

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5811-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5811-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5811-94:
(6*5)+(5*8)+(4*1)+(3*1)+(2*9)+(1*4)=99
99 % 10 = 9
So 5811-94-9 is a valid CAS Registry Number.

5811-94-9SDS

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 octahydro-4a,8a-epoxynaphthalene

1.2 Other means of identification

Product number -
Other names 4A,8a-epoxy-decahydro-naphthalene

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:5811-94-9 SDS

5811-94-9Downstream Products

5811-94-9Relevant articles and documents

Bipyridine N,N'-dioxide: A felicitous ligand for methyltrioxorhenium- catalyzed epoxidation of olefins with hydrogen peroxide

Nakajima, Makoto,Sasaki, Yuka,Iwamoto, Hatsue,Hashimoto, Shun-Ichi

, p. 87 - 88 (2007/10/03)

Methyltrioxorhenium-catalyzed oxidation of olefins with hydrogen peroxide in the presence of bipyridine N.N'-dioxide gave epoxides in high yields, with no sign of formation of hydrolyzed diols.

Catalytic Epoxidation of Alkenes with Oxone

Denmark, Scott E.,Forbes, David C.,Hays, David S.,DePue, Jeffrey S.,Wilde, Richard G.

, p. 1391 - 1407 (2007/10/02)

A practical, general and efficient protocol for the catalytic epoxidation of alkenes has been developed.The in situ generation of reactive dioxiranes capable of epoxidizing a variety of alkenes under biphasic conditions has been accomplished using phase transfer catalysts bearing a carbonyl group.Optimal epoxidation conditions employ 10 mol percent of 1-dodecyl-1-methyl-4-oxopiperidinium triflate (8d(+)OTf(-)) in a CH2Cl2/pH 7.5-8.0 biphase using potassium monoperoxosulfate (Oxone) as the oxidant.Optimization of the conditions identified (1) slow addition rate, (2) pH 7.5-8.0, (3) N-dodecyl chain, and (4) the triflate salt as key experimental and structural variables.A selection of nine olefins was successfully oxidized to the corresponding epoxides in 83-96percent yield.

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