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30385-19-4

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30385-19-4 Usage

Chemical classification

Alcohol

Carbon atoms

Eight

Carbon atom arrangement

Linear chain

Double bond

Between the first and second carbon atoms

Hydroxyl group

At the third position

Alcohol type

Primary alcohol

Industrial applications

Solvent, intermediate in manufacturing chemical products

Use in production

Fragrances and flavorings

Potential applications

Organic synthesis for complex chemicals

Role in industry

Significant, with various applications in different fields

Check Digit Verification of cas no

The CAS Registry Mumber 30385-19-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,8 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 30385-19:
(7*3)+(6*0)+(5*3)+(4*8)+(3*5)+(2*1)+(1*9)=94
94 % 10 = 4
So 30385-19-4 is a valid CAS Registry Number.

30385-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name octa-1,7-dien-3-ol

1.2 Other means of identification

Product number -
Other names 3-hydroxy-1,7-octadiene

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:30385-19-4 SDS

30385-19-4Upstream product

30385-19-4Relevant articles and documents

Imidazolium salts and the use of these ionic liquids as a solvent and as a catalyst

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Example 16, (2008/06/13)

New 1,2,3- or 1,2,3,4- or 1,2,3,4,5- substituted imidazolium salts and their uses as solvent in catalyzed organic reactions, as well as compositions containing them and a transition metal compound. They can be used in the following reactions : the telomerisation of conjugated dienes, the dimerisation of olefins, the oligomerisation of olefins, the polymerization of olefins, the alkylation of olefins, the hydrogenation of olefins, the olefin metathesis, the hydroformylation of olefins, the ring-closing metathesis of olefins, the ring-opening metathesis polymerisation of olefins, the symetric or asymetric epoxidation of olefins (including heteroatom substituted olefins) and the cyclopropanation of olefins, the condensation reaction, the hydrogenation reaction, the isomerization reaction, the Suzuki cross-coupling reactions, the amination reaction, the partial oxidation of alkancs, the kinetic resolution of racemic mixtures, the hydrogenation of imines, the hydrogenation of ketones, the transfer hydrogenation and the hydroxylation of aromatic organic compounds.

SYNTHESIS OF UNSATURATED ALCOHOLS BY TELOMERIZATION OF H2O WITH 1,3-DIENES, CATALYSED BY PALLADIUM COMPLEXES

Dzhemilev, U. M.,Sidorova, V. V.,Kunakova, R. V.

, p. 525 - 529 (2007/10/02)

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