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CAS

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135014-05-0

4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 4-Chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane

    Cas No: 135014-05-0

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  • 135014-05-0 Structure

  • Basic information

    1. Product Name: 4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane
    2. Synonyms: 1,3-dioxolane, 4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-; 4-Chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane
    3. CAS NO:135014-05-0
    4. Molecular Formula: C5ClF9O2
    5. Molecular Weight: 298.4909
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135014-05-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 80°C at 760 mmHg
    3. Flash Point: 2.2°C
    4. Appearance: N/A
    5. Density: 1.79g/cm3
    6. Vapor Pressure: 96.3mmHg at 25°C
    7. Refractive Index: 1.316
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane(135014-05-0)
    12. EPA Substance Registry System: 4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane(135014-05-0)

  • 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: 135014-05-0(Hazardous Substances Data)

135014-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135014-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,1 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 135014-05:
(8*1)+(7*3)+(6*5)+(5*0)+(4*1)+(3*4)+(2*0)+(1*5)=80
80 % 10 = 0
So 135014-05-0 is a valid CAS Registry Number.

135014-05-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolane,4-chloro-4,5,5-trifluoro-2,2-bis(trifluoromethyl)

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:135014-05-0 SDS

135014-05-0Downstream Products

135014-05-0Relevant articles and documents

A preparation method for halogenated 2,2-bis(perfluoro substituent)-1,3-dioxolane type compounds

-

Paragraph 0043; 0044; 0046; 0047; 0048-0061; 0062; 0063, (2017/12/09)

A gaseous-phase preparation method for halogenated 2,2-bis(perfluoro substituent)-1,3-dioxolane type compounds is disclosed. The method includes, reacting 2,2-bis(perfluoro substituent)-1,3-dioxolane with Cl2 and HF with the existence of a catalyst to obtain a corresponding halogenated 2,2-bis(perfluoro substituent)-1,3-dioxolane. The method can achieve a one-step reaction, and has characteristics of simple process steps, simple equipment, low energy consumption, and small amounts of the three wastes. The prepared halogenated 2,2-bis(perfluoro substituent)-1,3-dioxolane compounds are suitable for use as a polymerization monomer.

Thermal Decomposition of Fluorinated Dioxolane Carboxylates

Hung, Ming-H.,Farnham, William B.

, p. 563 - 570 (2007/10/02)

Synthesis of fluorodioxole olefin monomers by thermal decomposition of fluorinated dioxolane carboxylic acid and the corresponding acyl chloride was explored.Complex product formation is observed, including acyl fluoride from C1-F exchange, the hydro-dioxolane from proton abstraction, the cyclic ether ketone from dioxolane ring opening, and the epoxy acid fluoride from thermal rearrangement.The product distribution is strongly dependent upon reaction conditions.The main influential factors include the reaction temperature, the base used for the reaction, the presence or absence of solvent, and the counter ion associated with the intermediate salt.A mechanism is proposed to rationalize both the results and the product distribution.Methods to make authentic samples for product analysis are reported. Key Words Fluorine; Dioxolane; Dioxole; Thermal decomposition; Pyrolysis; Acid halide; Carboxylate; Fluoroolefin; Heterocyclic; Fluorocarbon.

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