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Pentyl vinyl ether, also known as 1-pentyl vinyl ether or 1-ethenylpentane, is an organic compound with the chemical formula C7H14O. It is a colorless, flammable liquid that is soluble in most organic solvents. Pentyl vinyl ether is primarily used as a chemical intermediate in the synthesis of various polymers, pharmaceuticals, and other specialty chemicals. It is produced through the reaction of 1-pentanol with vinyl chloride or vinyl acetate. Due to its reactivity, it is often used in the production of copolymers and homopolymers, which have applications in coatings, adhesives, and elastomers. Additionally, it can be used as a solvent or a reagent in various chemical reactions.

5363-63-3

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5363-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5363-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5363-63:
(6*5)+(5*3)+(4*6)+(3*3)+(2*6)+(1*3)=93
93 % 10 = 3
So 5363-63-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O/c1-3-5-6-7-8-4-2/h4H,2-3,5-7H2,1H3

5363-63-3SDS

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-ethenoxypentane

1.2 Other means of identification

Product number -
Other names Vinyl-n-pentylaether

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:5363-63-3 SDS

5363-63-3Relevant academic research and scientific papers

Use of Iridium-Catalyzed Transfer Vinylation for the Synthesis of Bio-Based (bis)-Vinyl Ethers

Beck, Horst,Brandt, Adrian,Grauke, Reni,Jiao, Haijun,Kubis, Christoph,Spannenberg, Anke,Spiegelberg, Brian,Taden, Andreas,Tin, Sergey,de Vries, Johannes G.

, (2022/02/10)

The iridium catalyzed transfer vinylation of bio-based polyols and of other alcohols and phenols with interesting structural motifs was accomplished with vinyl acetate in 2-MeTHF as a green solvent. The optimized synthetic procedure has as main advantages the use of catalytic instead of stoichiometric amounts of base and high selectivities towards the formation of bis-vinyl ethers as a result of the suppression of the acetal formation reaction that typically occurs in the vinylation of diols. In addition, the thermodynamically preferred transesterification reaction leading to the acetate esters and bis-esters was completely suppressed. DFT calculations revealed an iridium-acetate complex as the active catalytic species and they disclosed the importance of the carbonyl group of vinyl acetate for the formation of a six-membered cyclic intermediate.

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