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perfluoro-β-methylstyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111302-04-6 Structure
  • Basic information

    1. Product Name: perfluoro-β-methylstyrene
    2. Synonyms: perfluoro-β-methylstyrene
    3. CAS NO:111302-04-6
    4. Molecular Formula:
    5. Molecular Weight: 298.083
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111302-04-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: perfluoro-β-methylstyrene(CAS DataBase Reference)
    10. NIST Chemistry Reference: perfluoro-β-methylstyrene(111302-04-6)
    11. EPA Substance Registry System: perfluoro-β-methylstyrene(111302-04-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 111302-04-6(Hazardous Substances Data)

111302-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111302-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,3,0 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 111302-04:
(8*1)+(7*1)+(6*1)+(5*3)+(4*0)+(3*2)+(2*0)+(1*4)=46
46 % 10 = 6
So 111302-04-6 is a valid CAS Registry Number.

111302-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name perfluoro-β-methylstyrene

1.2 Other means of identification

Product number -
Other names Perfluoro-1-phenylpropene-1

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:111302-04-6 SDS

111302-04-6Relevant articles and documents

Electrophilic reactions of fluorocarbons under the action of aluminum chlorofluoride, a potent Lewis acid

Petrov, V. A.,Krespan, C. G.,Smart, B. E.

, p. 138 - 142 (2007/10/03)

A new Lewis acid - aluminum chlorofluoride - was demonstrated to be an effective catalyst for the isomerisation of fluoroolefins, polyfluorinated epoxides and cyclopropanes.At ambient temperature this catalyst converts perfluorobutadiene-1,3 into perfluorobutyne-2 and perfluoro(4-methylpentene-2) into perfluoro(2-methylpentene-2) in nearly quantitative yield.At 100 deg C, aluminum chlorofluoride causes the cleavage of perfluorinated tertiary amines. - Keywords: Electrophilic reactions; Fluorocarbons; Aluminum chlorofluoride; Lewis acid; NMR spectroscopy

FLUORINATION OF POLYHALOGENATED UNSATURATED COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Bardin, V. V.,Avramenko, A. A.,Furin, G. G.,Krasilnikov, V. A.,Karelin, A. I.,et al.

, p. 385 - 400 (2007/10/02)

Vanadium pentafluoride reacts with polyfluorinated and polychlorinated olefins, alkadienes, cycloalkenes and cyclodienes in CFCl3 or without a solvent at -25 deg C to 100 deg C, forming products of addition of two fluorine atoms across the C=C bond.

INTRODUCTION OF A PENTAFLUOROPHENYL GROUP INTO PERFLUORINATED OLEFINS BY MEANS OF TRIMETHYLSILYLPENTAFLUOROBENZENE IN THE PRESENCE OF CESIUM FLUORIDE

Bardin, V. V.,Petrov, V. A.,Stennikova, I. V.,Furin, G. G.

, p. 46 - 49 (2007/10/02)

Trimethylsilylpentafluorobenzene reacts with terminal and internal perfluorinated olefins in the presence of cesium fluoride, forming perfluorinated phenylalkenes.

AN UNUSUAL TRANSFORMATION OF PERFLUORINATED 1- AND 3-PHENYLPROPENES TO POLYFLUOROCHLOROINDANES BY THE ACTION OF AlCl3

Platonov, V. E.,Dvornikova, K. V.

, p. 2617 - 2619 (2007/10/02)

The reaction of perfluorinated 1- and 3-phenylpropenes with AlCl3 gives polyfluorochloroindanes as the result of an intramolecular cyclization, apparently by an electrophilic pathway.

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