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Hexanediol monovinyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27336-16-9

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27336-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27336-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,3 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27336-16:
(7*2)+(6*7)+(5*3)+(4*3)+(3*6)+(2*1)+(1*6)=109
109 % 10 = 9
So 27336-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O2/c1-2-10-8-6-4-3-5-7-9/h2,9H,1,3-8H2

27336-16-9SDS

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 Hexanediol monovinyl ether

1.2 Other means of identification

Product number -
Other names 1,6-hexanediol vinyl ether

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:27336-16-9 SDS

27336-16-9Downstream Products

27336-16-9Relevant academic research and scientific papers

METHOD OF PRODUCING VINYL ETHER, AND CATALYST FOR ETHER EXCHANGE REACTION

-

Paragraph 0140, (2017/08/14)

PROBLEM TO BE SOLVED: To provide a method for producing vinyl ether that allows a reaction to sufficiently proceed even in a small amount of catalyst, and facilitates the recovery and reuse of the catalyst with excellent operability. SOLUTION: A method for producing vinyl ether represented by formula (3) is characterized in that alcohol and vinyl ether represented by formula (2) are subjected to ether replacement reaction. There is also provided catalyst that comprises a metal nano cluster obtained by heating a transition metal compound in solvent comprising coordination organic solvent and a nitrogen-containing heterocyclic compound. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Au(I) complexes-catalyzed transfer vinylation of alcohols and carboxylic acids

Nakamura, Aki,Tokunaga, Makoto

, p. 3729 - 3732 (2008/09/20)

Au(I) complexes-catalyzed transfer vinylation of alcohols and carboxylic acids has been achieved. The catalyst system consists of 2 mol % AuClPPh3 and 2 mol % AgOAc. Primary alcohols and secondary alcohols were converted into corresponding vinyl ethers in good yield (64-93%); however, tertiary alcohols showed poor reactivities. Carboxylic acids were also transformed into corresponding vinyl esters in good yield (78-96%).

Process for producing vinyl ether compounds

-

, (2008/06/13)

A process produces vinyl ether compounds and includes allowing a vinyl ester compound represented by following Formula (1): 1wherein R1, R2, R3 and R4 are the same or different and are each a hydrogen atom or an organic group, to react with a hydroxy compound represented by following Formula (2):R5OH??(2)wherein R5 is an organic group, in the presence of at least one transition element compound to thereby yield a vinyl ether compound represented by following Formula (3): 2wherein R2, R3, R4 and R5 have the same meanings as defined above. Such transition element compounds include iridium compounds and other compounds containing Group VIII elements.

Development of a highly efficient catalytic method for synthesis of vinyl ethers

Okimoto, Yoshio,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 1590 - 1591 (2007/10/03)

A new method for the preparation of alkyl vinyl ethers has been developed. Thus, various types of alkyl vinyl ethers were synthesized by the reaction of alcohols with vinyl acetate under the influence of a catalytic amount of [Ir(cod)Cl]2 combined with Na2CO3 in good to excellent yields. Copyright

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