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926-02-3

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926-02-3 Usage

Chemical Properties

liquid

Uses

tert-Butyl vinyl ether is used in the synthesis of 3-tert-Butoxycyclobutanone by reacting with ketene using zinc(II) chloride as a catalyst. It acts as an intermediate for the functional vinyl monomer.

Check Digit Verification of cas no

The CAS Registry Mumber 926-02-3 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 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 926-02:
(5*9)+(4*2)+(3*6)+(2*0)+(1*2)=73
73 % 10 = 3
So 926-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-5-7-6(2,3)4/h5H,1H2,2-4H3

926-02-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H30770)  tert-Butyl vinyl ether, 98%, stab. with ca 0.1% N,N-diethylaniline   

  • 926-02-3

  • 5g

  • 476.0CNY

  • Detail
  • Alfa Aesar

  • (H30770)  tert-Butyl vinyl ether, 98%, stab. with ca 0.1% N,N-diethylaniline   

  • 926-02-3

  • 25g

  • 1441.0CNY

  • Detail
  • Aldrich

  • (410012)  tert-Butylvinylether  98%

  • 926-02-3

  • 410012-10ML

  • 1,251.90CNY

  • Detail
  • Aldrich

  • (410012)  tert-Butylvinylether  98%

  • 926-02-3

  • 410012-50ML

  • 4,320.81CNY

  • Detail

926-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name TERT-BUTYL VINYL ETHER

1.2 Other means of identification

Product number -
Other names 2-ethenoxy-2-methylpropane

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:926-02-3 SDS

926-02-3Relevant articles and documents

-

Bamkole,T.O.,Emovon,E.U.

, p. 332 - 333 (1968)

-

Method for producing alkenyl ethers

-

, (2008/06/13)

Alkenyl ethers are prepared by reacting the corresponding alcohols or phenols with acetylenes in the liquid phase in the presence of basic alkali metal compounds and a cocatalyst comprising compounds of the formula (Ia) and/or (Ib) R1O—(CH2CH2CH2CH2O)n—H??(Ia) R1O—(CH2CH2CH2CH2O)n—H2,??(Ia) where R1, R2 are, independently of one another, C1-C6-alkyl or C2-C6-alkenyl, or R1 and R2 together form a butyl unit and n is 1, 2, 3, 4 or 5.

17O NMR Spectra of Vinyl Ethers

Taskinen, Esko,Hellman, Jaakko

, p. 353 - 357 (2007/10/02)

The 17O spectra of 58 α,β-unsaturated (vinyl) ethers were recorded in CDCl3 solution.The dependence of the chemical shift on the number and position of alkyl substituents in the vinyl moiety and on the nature and bulkiness of the alkoxy group was explored.The oxygen chemical shifts proved to be sufficiently sensitive to structural factors to make 17O NMR spectroscopy a useful tool in the investigation of the electronic and spatial syructures of vinyl ethers. - Keywords: NMR 17O NMR Vinyl ethers

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