2354-06-5

Basic information

• Product Name: CFC-213
• Synonyms: CFC-213;Propane11133-pentachloro-223-trifluoro-;Chlorofluorocarbon-213 (CFC-213, R-213);1,1,1,3,3-Pentachloro-2,2,3-trifluoropropane
• CAS NO: 2354-06-5
• Molecular Formula: C₃Cl₅F₃
• Molecular Weight: 270.29
• Product Categories: refrigerants
• Mol File: 2354-06-5.mol

Chemical Properties

• Boiling Point: 156.25°C
• Flash Point: 54.5°C
• Appearance: /
• Density: 1.7483 (estimate)
• Vapor Pressure: 5.43mmHg at 25°C
• Refractive Index: 1.4805 (estimate)
• CAS DataBase Reference: CFC-213(CAS DataBase Reference)
• NIST Chemistry Reference: CFC-213(2354-06-5)
• EPA Substance Registry System: CFC-213(2354-06-5)

Safety Data

• Hazardous Substances Data: 2354-06-5(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 14, p. 887, 1973 DOI: 10.1016/S0040-4039(00)72443-9

InChI:InChI=1/C3Cl5F3/c4-2(5,6)1(9,10)3(7,8)11

Upstream product

• 56-23-5 tetrachloromethane 
• 79-38-9 Chlorotrifluoroethylene 
• 79-35-6 1,1'-dichloro-2,2'-difluoroethene 
• 422-52-6 1,1,3,3-tetrachloro-1,2,2-trifluoropropane 
• 75-69-4 trichlorofluoromethane 
• 422-50-4 1,1,1,3-tetrachloro-2,2,3-trifluoropropane 
• 3182-26-1 1,1,1,3,3,3-hexachloro-2,2-difluoro-propane 

Downstream Products

• 3182-26-1 1,1,1,3,3,3-hexachloro-2,2-difluoro-propane 
• 75-00-3 chloroethane 
• 78-38-6 ethylphosphonic acid diethyl ester 
• 815-16-7 1,1,3,3-tetrachloro-2,3-difluoro-propene 
• 78-40-0 triethyl phosphate 

Relevant articles and documents

Synthese des α,ω-dichlorures d'acide a chaines chlorofluorees par hydrolyse des α,ω-bis trichloromethyles correspondants

This paper describes the transformation of α,ω-bis(trichloromethyl) compounds into perhalogenated diacid chlorides.The general formulae of the starting products are CCl3-(CF2-CFCl)x-CF2-CCl3 (I,x) with x=0, 1, 2 and CCl3-CF2-CCl2-CF2-CCl3 (II).Hydrolysis, by oleum, of compounds (I,0) and (I, 2) leads to the corresponding diacid chlorides.Hydrolysis of (I, 1) and (II) however yields perhalogenated cyclic, sixmembered stable acid anhydrides.In the second part of this work, several methods are compared for synthesizing diacid chlorides from diacids or cyclic anhydride s prepared by the hydrolysis of (I, 1) and (II).We have found that of these the most interesting is the reaction between a perhalogenated diacid with 1,4-bis(trichloromethyl)benzene.The perhalogenated diacid chlorides are prepared with a minimum yield of 50percent.