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13294-31-0

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13294-31-0 Usage

Description

[(Z)-2-ethoxyethenyl]benzene, also known as styrene oxide, is a colorless organic compound with a molecular formula of C10H10O. It is a derivative of styrene and is recognized for its applications in the production of various polymers, resins, and other chemical products.

Uses

Used in Polymer and Resin Production:
[(Z)-2-ethoxyethenyl]benzene is used as a chemical intermediate for the manufacturing of polystyrene, a versatile plastic material. Polystyrene is widely utilized in the production of packaging materials, insulation, and a range of consumer goods due to its favorable properties such as clarity, rigidity, and resistance to water and electricity.
Used in Plastics and Elastomers:
Styrene oxide serves as a crosslinking agent in the production of various plastics and elastomers, enhancing their structural integrity, durability, and performance characteristics. This application is particularly relevant in industries where materials are subjected to mechanical stress or require increased resistance to environmental factors.
Used in Pharmaceutical and Agricultural Chemical Synthesis:
[(Z)-2-ethoxyethenyl]benzene is also employed as a key component in the synthesis of certain pharmaceuticals and agricultural chemicals, highlighting its versatility and importance in the chemical industry.
It is crucial to handle and use [(Z)-2-ethoxyethenyl]benzene with caution, as it is a toxic substance that can cause irritation to the skin, eyes, and respiratory system. Proper safety measures and guidelines should be followed to minimize potential health risks during its production and application.

Check Digit Verification of cas no

The CAS Registry Mumber 13294-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13294-31:
(7*1)+(6*3)+(5*2)+(4*9)+(3*4)+(2*3)+(1*1)=90
90 % 10 = 0
So 13294-31-0 is a valid CAS Registry Number.

13294-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-2-ethoxyethenyl]benzene

1.2 Other means of identification

Product number -
Other names cis-Styryl ethyl 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:13294-31-0 SDS

13294-31-0Relevant articles and documents

Base-promoted stereoselective hydroalkoxylation of alkynes

Patel, Monika,Sushmita,Verma, Akhilesh Kumar

, p. 169 - 175 (2018/09/14)

Base-promoted and stereoselective synthesis of C(sp2)-O bond through the anti-Markovnikov addition of alcohols onto alkyne and has been discovered. Developed protocol tolerates a wide variety of functional groups to afford styryl ethers from commercially

Intermolecular Hydroalkoxylation of Terminal Alkynes Catalyzed by a Dipyrrinato Rhodium(I) Complex with Unusual Selectivity

Lam, Raphael H.,Walker, D. Barney,Tucker, Matthew H.,Gatus, Mark R. D.,Bhadbhade, Mohan,Messerle, Barbara A.

supporting information, p. 4312 - 4317 (2015/09/22)

An operationally simple and atom-economical method for the E-selective preparation of enol ethers is described. A novel dicarbonyl(5-phenyldipyrrinato)rhodium complex, 2, was prepared in four synthetic steps, characterized by X-ray crystallography and NMR

Synthesis of chiral acetals by asymmetric selenenylations

Uehlin, Lars,Wirth, Thomas

experimental part, p. 1374 - 1385 (2010/03/03)

Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficient synthesis of such compounds including the determination of their absolute configuration is described.

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