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929-62-4

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929-62-4 Usage

General Description

1-(vinyloxy)octane, also known as vinyl octyl ether, is a chemical compound with the formula C10H20O. It is a clear, colorless liquid with a slightly fruity odor. 1-(vinyloxy)octane is primarily used as a reactive diluent in the production of epoxy resins, where it acts as a modifier to improve flexibility and impact resistance. It is also used as an intermediate in the synthesis of other organic compounds, and as a solvent in various chemical processes. While 1-(vinyloxy)octane has low acute toxicity, inhalation or skin contact with the substance may cause irritation. It is important to handle and store 1-(vinyloxy)octane carefully to minimize potential health and safety risks.

Check Digit Verification of cas no

The CAS Registry Mumber 929-62-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 929-62:
(5*9)+(4*2)+(3*9)+(2*6)+(1*2)=94
94 % 10 = 4
So 929-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-3-5-6-7-8-9-10-11-4-2/h4H,2-3,5-10H2,1H3

929-62-4SDS

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 1-ethenoxyoctane

1.2 Other means of identification

Product number -
Other names n-octyl 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:929-62-4 SDS

929-62-4Relevant articles and documents

Calcium Carbide Looping System for Acetaldehyde Manufacturing from Virtually any Carbon Source

Rodygin, Konstantin S.,Lotsman, Kristina A.,Ananikov, Valentine P.

, p. 3679 - 3685 (2020/06/17)

A vinylation/devinylation looping system for acetaldehyde manufacturing was evaluated. Vinylation of iso-butanol with calcium carbide under solvent-free conditions was combined with hydrolysis of the resulting iso-butyl vinyl ether under slightly acidic conditions. Acetaldehyde produced by hydrolysis was collected from the reaction mixture by simple distillation, and the remaining alcohol was redirected to the vinylation step. All the inorganic co-reagents can be looped as well, and the full sequence is totally sustainable. A complete acetaldehyde manufacturing cycle was proposed on the basis of the developed procedure. The cycle was fed with calcium carbide and produced the aldehyde as a single product in a total preparative yield of 97 %. No solvents, hydrocarbons, or metal catalysts were needed to maintain the cycle. As calcium carbide in principle can be synthesized from virtually any source of carbon, the developed technology represents an excellent example of biomass and waste conversion into a valuable industrial product.

Competition between reaction and intramolecular energy redistribution in solution: Observation and nature of nonstatistical dynamics in the ozonolysis of vinyl ethers

Quijano, Larisa Mae M.,Singleton, Daniel A.

supporting information; experimental part, p. 13824 - 13827 (2011/10/12)

Experimental product ratios in ozonolyses of alkyl vinyl ethers in solution do not fit with expectations based on statistical rate theories. The selectivity among cleavage pathways increases with the size of the alkyl group but to an extent that is far less than RRKM theory would predict. Trajectory studies account for the observed selectivities and support a mechanism involving a competition between cleavage of the primary ozonide and intramolecular vibrational energy redistribution. A statistical model is presented that assumes that RRKM theory holds for a molecular subset of the primary ozonides, allowing the rates of energy loss from the ozonides to be estimated from the observed product ratios.

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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