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1,1,3,3-Tetrachloro-1,2,2,3-tetrafluoropropane, also known as CCl2FCF2CCl3 or R-114, is a chlorofluorocarbon (CFC) compound that was primarily used as a refrigerant and as a propellant in aerosol products. It is a colorless, volatile liquid with a low boiling point and high chemical stability. Due to its high ozone depletion potential (ODP) and global warming potential (GWP), its production and use have been phased out under the Montreal Protocol to protect the ozone layer and mitigate climate change.

2354-04-3

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2354-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2354-04-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2354-04:
(6*2)+(5*3)+(4*5)+(3*4)+(2*0)+(1*4)=63
63 % 10 = 3
So 2354-04-3 is a valid CAS Registry Number.

2354-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3-tetrachloro-1,2,2,3-tetrafluoropropane

1.2 Other means of identification

Product number -
Other names 1,1,3,3-tetrachloro-1,2,2,3-tetrafluoro-propane

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:2354-04-3 SDS

2354-04-3Relevant academic research and scientific papers

Thermal chlorofluorination of propyne and propadiene

Belter, Randolph K.

, p. 1611 - 1615 (2008/09/18)

Propyne and propadiene have been found to readily undergo vapor phase catalyzed chlorofluorination. At temperatures to 285 °C, the reaction forms mixtures of C3F4Cl4 isomers that differ in composition from mixtures obtained from either propane or propene.

Synthesis of > and Some Chlorofluoropropenes

Paleta, Oldrich,Kvicala, Jaroslav,Guenter, Jaroslav,Dedek, Vaclav

, p. 920 - 924 (2007/10/02)

The starting substances C3Cl5F3 (1) and C3Cl4F4 (2) prepared earlier by the addition of CCl3F with CClF=CClF and/or CF2=CClF were utilized for the synthesis of chlorofluoropropenes by means of fluorination, reduction of C-Cl bonds in halogenopropanes, and final dehalogenation, all the reactions being performed at atmospheric pressure.The reaction conditions permit laboratory scale production.The contents of the isomeric admixtures in the resultant products were determined by NMR spectroscopy.The starting halogenopropanes 1, 2 represent mixtures of isomers, but in course of the individual synthetic steps the content of the main isomer was generally increased.In comparison with previously used syntheses, our procedure proves advantageous for the synthesis of "perfluoroallylchloride" (9a, isomer purity 95percent).Using this procedure a number of halogenopropanes were prepared and dechlorinated to give the corresponding halogenopropenes (isomer purity percent): CClF2-CClF-CCl2F (2a, 87), CF3-CClF-CCl3 (2b, 78), CClF2-CClF-CClF2 (3a, 87), CF3-CClF-CCl2F (3b, 90), CF3-CClF-CHCl2 (5a, 90), CF3-CClF-CHClF (6a, 73), CClF2-CF=CClF (8a, 93), CF3-CF=CCl2 (8b, 84), 9a, CF3-CF=CClF (9b, 86) and CF3-CF=CHCl (11a, 84).The minor isomers in substance 2 yielded products which were isolated after being combined from several preparations: CClF2-CF2-CHCl2 (5b, 84); CClF2-CF=CHCl (10a, 98), which by addition of chlorine yielded CClF2-CClF-CHCl2 (4a, 95).The NMR spectra of all the major and minor products, excluding perhalogenopropanes, are listed.

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