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Vinyl cyclohexanecarboxylate, also known as 3-cyclohexene-1-carboxylic acid, vinyl ester, is a colorless liquid organic compound with the chemical formula C9H14O2. It is derived from the reaction of cyclohexanecarboxylic acid with acetylene, resulting in a vinyl ester. vinyl cyclohexanecarboxylate is primarily used as a monomer in the production of specialty polymers and resins, which possess unique properties such as high chemical resistance, low temperature flexibility, and excellent adhesion. These polymers find applications in various industries, including coatings, adhesives, and composite materials. Vinyl cyclohexanecarboxylate is also known for its low toxicity and environmental friendliness, making it a preferred choice in eco-friendly product development.

4840-76-0

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4840-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4840-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4840-76:
(6*4)+(5*8)+(4*4)+(3*0)+(2*7)+(1*6)=100
100 % 10 = 0
So 4840-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-2-11-9(10)8-6-4-3-5-7-8/h2,8H,1,3-7H2

4840-76-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethenyl cyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names cyclohexanecarboxylic acid vinyl ester

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:4840-76-0 SDS

4840-76-0Downstream Products

4840-76-0Relevant academic research and scientific papers

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 Preparing Vinyl Carboxylates

-

Page/Page column 6, (2009/01/24)

The present invention relates to a process for preparing vinyl carboxylates, wherein a carboxylic acid is reacted with an alkyne compound in the presence of a catalyst which is selected from carbonyl complexes, halides and oxides of rhenium, of manganese, of tungsten, of molybdenum, of chromium and of iron and rhenium metal at a temperature of ≦300° C. The process gives the desired vinyl esters with high yield.

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