Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1717-00-6

Post Buying Request

1717-00-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1717-00-6 Usage

Chemical Properties

colourless liquid

Uses

HCFC 141b has been developed as a substitute for the fully halogenated chlorofluorocarbons, mainly for use as a blowing agent for polyurethane and polyisocyanate insulating foams and as a solvent in electronic and other precision cleaning applications. It is viewed as an interim compound, and production will be phased out beginning in 2003.

General Description

Colorless liquid at ambient conditions.

Reactivity Profile

Dichlorofluoroethane may be incompatible with strong oxidizing and reducing agents. May be incompatible with some amines, nitrides, azo/diazo compounds, alkali metals, and epoxides. An explosion occurred when an emptied drum of Dichlorofluoroethane was cut into by a grinder; may be more flammable than once thought.

Carcinogenicity

A 2 year inhalation study was conducted during which four groups of 80 male and 80 female rats were exposed to levels of 0, 1500, 5000, and 15,000–20,000 ppm, 6 h/day, 5 days/week. The high exposure level was increased from 15,000 to 20,000 ppm after 4 months since no signs of toxicity were seen at 15,000 ppm. At the end of 2 years, an increased incidence of benign Leydig cell tumors and Leydig cell hyperplasia was seen in the male rats 5000 and 20,000 ppm, but not at 1500 ppm. These tumors are common in the aging rat and did not follow an exposure related pattern. They are not considered to be a risk factor for humans. No other treatment related effects were seen.

Check Digit Verification of cas no

The CAS Registry Mumber 1717-00-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1717-00:
(6*1)+(5*7)+(4*1)+(3*7)+(2*0)+(1*0)=66
66 % 10 = 6
So 1717-00-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H11F3O3/c1-2-18-11(17)7-10(16)8-4-3-5-9(6-8)12(13,14)15/h3-6H,2,7H2,1H3

1717-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Dichlorofluoroethane

1.2 Other means of identification

Product number -
Other names HFC141B

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:1717-00-6 SDS

1717-00-6Synthetic route

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With hydrogen fluoride; SbCl5 on Carbon at 100℃; under 760.051 Torr; for 0.00277778h;A 80%
B n/a
C n/a
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With hydrogen fluoride at 150℃; unter Druck;
With antimony(III) fluoride at 150℃; unter Druck;
With antimony dichloride trifluoride; antimony(III) fluoride anfangs unter Kuehlung mit Eis;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With hydrogen fluoride at 65℃;
With hydrogen fluoride; tin(IV) chloride
With hydrogen fluoride Heating;
With hydrogen fluoride
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

A

4-chloro-6-methyl-2H-pyran-2-one
17422-72-9

4-chloro-6-methyl-2H-pyran-2-one

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

D

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

E

3,5-dichlorophenol
591-35-5

3,5-dichlorophenol

F

2-methyl-5,7-dichlorochromone

2-methyl-5,7-dichlorochromone

Conditions
ConditionsYield
With sulfuric acid; hydrogen fluoride; antimonypentachlorideA 1.19 g
B n/a
C n/a
D n/a
E 0.20 g
F 0.08 g
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

D

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

Conditions
ConditionsYield
With fluorinated (with SF4) γ-alumina; hydrogen fluoride for 2h; Product distribution; Ambient temperature;
With hydrogen fluoride; antimonypentachloride at 60℃; under 7500.6 Torr; Mechanism; var. reaction partners and temp.;
With chromium(III) oxide; sulfur tetrafluoride; hydrogen fluoride at 20℃; for 2h; Product distribution; Further Variations:; Reagents;
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

D

Vinylidene fluoride
75-38-7

Vinylidene fluoride

Conditions
ConditionsYield
With fluorinated Fe3O4 for 2h; Ambient temperature; Yields of byproduct given. Title compound not separated from byproducts;
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

A

HCFC-141b
1717-00-6

HCFC-141b

B

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

Conditions
ConditionsYield
With fluorinated Co3O4 for 2h; Ambient temperature; Yields of byproduct given. Title compound not separated from byproducts;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

A

1,1,1-Trichloro-2,2,2-trifluoroethane
354-58-5

1,1,1-Trichloro-2,2,2-trifluoroethane

B

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

C

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

D

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With fluorinated Co3O4 for 2h; Ambient temperature; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

A

1,1,1-Trichloro-2,2,2-trifluoroethane
354-58-5

1,1,1-Trichloro-2,2,2-trifluoroethane

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

D

1,1,2-Trichloro-1,2,2-trifluoroethane
76-13-1

1,1,2-Trichloro-1,2,2-trifluoroethane

Conditions
ConditionsYield
With fluorinated Co3O4 for 2h; Ambient temperature; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

A

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

B

HCFC-141b
1717-00-6

HCFC-141b

C

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

D

1,2-dichloro-1,1-difluoroethane
1649-08-7

1,2-dichloro-1,1-difluoroethane

Conditions
ConditionsYield
With fluorinated Fe3O4 for 2h; Ambient temperature; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

A

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

B

HCFC-141b
1717-00-6

HCFC-141b

C

1,2-dichloro-1,1-difluoroethane
1649-08-7

1,2-dichloro-1,1-difluoroethane

D

1,1,2-Trichloro-1,2,2-trifluoroethane
76-13-1

1,1,2-Trichloro-1,2,2-trifluoroethane

Conditions
ConditionsYield
With fluorinated Fe3O4 for 2h; Ambient temperature; Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
1,1,3,3-tetrachloro-1,3-difluoro-2-propanone
79-51-6

1,1,3,3-tetrachloro-1,3-difluoro-2-propanone

acetone
67-64-1

acetone

A

Dichlorofluoromethane
75-43-4

Dichlorofluoromethane

B

HCFC-141b
1717-00-6

HCFC-141b

C

trichlorofluoromethane
75-69-4

trichlorofluoromethane

D

1-chloro-1-fluoroethane
2317-91-1

1-chloro-1-fluoroethane

E

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

F

CFC-112a
76-12-0

CFC-112a

Conditions
ConditionsYield
With propene; sulphur hexafluoride for 0.5h; Rate constant; Ambient temperature; Irradiation; also with acetone-d6;
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

D

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

E

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

Conditions
ConditionsYield
With fluorinated indium(III) oxide Product distribution; Ambient temperature; further reagent: fluorinated gallium(III) oxide;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

A

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

B

HCFC-141b
1717-00-6

HCFC-141b

C

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

Conditions
ConditionsYield
With fluorinated gallium(III) oxide Product distribution; Ambient temperature;
1,1,2-Trichloro-1,2,2-trifluoroethane
76-13-1

1,1,2-Trichloro-1,2,2-trifluoroethane

A

1,1,1-Trichloro-2,2,2-trifluoroethane
354-58-5

1,1,1-Trichloro-2,2,2-trifluoroethane

B

HCFC-141b
1717-00-6

HCFC-141b

C

chlorotrifluoromethane
75-72-9

chlorotrifluoromethane

Conditions
ConditionsYield
With fluorinated gallium(III) oxide Product distribution; Ambient temperature; further reagent: fluorinated indium(III) oxide;
1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

hydrogen fluoride
7664-39-3

hydrogen fluoride

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

hydrogen fluoride
7664-39-3

hydrogen fluoride

antimonypentachloride
7647-18-9

antimonypentachloride

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

antimony(III) fluoride
7783-56-4

antimony(III) fluoride

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

chlorinated SbF3

chlorinated SbF3

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

HCFC-141b
1717-00-6

HCFC-141b

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

HF (4 mol)

HF (4 mol)

A

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

B

HCFC-141b
1717-00-6

HCFC-141b

C

1,1,1-trichloroethane
71-55-6

1,1,1-trichloroethane

Conditions
ConditionsYield
at 65℃; unter Druck;
dichloromethane
75-09-2

dichloromethane

A

pentaerythrityl tetrachloride
3228-99-7

pentaerythrityl tetrachloride

B

Isobutane
75-28-5

Isobutane

C

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

D

HCFC-141b
1717-00-6

HCFC-141b

E

1,2-dichloro-1,1-difluoroethane
1649-08-7

1,2-dichloro-1,1-difluoroethane

F

pentachloroethane
76-01-7

pentachloroethane

G

(ClCH2)3CCl

(ClCH2)3CCl

Conditions
ConditionsYield
With fluorinated gallium(III) oxide Product distribution; Mechanism; Ambient temperature;
1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

sodium phosphate

sodium phosphate

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With HF; TiCl4 In sulfolane; hydrogenchloride; polyethylene
With HF; TiCl4 In sulfolane; hydrogenchloride; polyethylene
CH3 -(CF=NH2)+

CH3 -(CF=NH2)+

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With HF
tantalum pentafluoride
7783-71-3

tantalum pentafluoride

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

HCFC-141b
1717-00-6

HCFC-141b

Conditions
ConditionsYield
With hydrogen fluoride In carbon dioxide
HCFC-141b
1717-00-6

HCFC-141b

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

Conditions
ConditionsYield
at 200℃; for 2h; Conversion of starting material;82%
1-hexene
592-41-6

1-hexene

HCFC-141b
1717-00-6

HCFC-141b

C8H15Cl2F

C8H15Cl2F

Conditions
ConditionsYield
With tris[(2-pyridylmethyl)amine]; copper(l) chloride In N,N-dimethyl-formamide at 130℃; for 14h;46%
HCFC-141b
1717-00-6

HCFC-141b

A

1-fluoroethane
353-36-6

1-fluoroethane

B

chloroethane
75-00-3

chloroethane

C

1-chloro-1-fluoroethane
1615-75-4

1-chloro-1-fluoroethane

Conditions
ConditionsYield
With hydrogen; platinum on activated charcoal at 200℃;A 45%
B 21%
C 31%
HCFC-141b
1717-00-6

HCFC-141b

oct-1-ene
111-66-0

oct-1-ene

C10H19Cl2F

C10H19Cl2F

Conditions
ConditionsYield
With tris[(2-pyridylmethyl)amine]; copper(l) chloride In N,N-dimethyl-formamide at 130℃; for 14h;45%
HCFC-141b
1717-00-6

HCFC-141b

acrylic acid methyl ester
292638-85-8

acrylic acid methyl ester

C6H9Cl2FO2

C6H9Cl2FO2

Conditions
ConditionsYield
With tris[(2-pyridylmethyl)amine]; copper(l) chloride In N,N-dimethyl-formamide at 130℃; for 14h;17%
chloroethylene
75-01-4

chloroethylene

HCFC-141b
1717-00-6

HCFC-141b

C4H6Cl3F

C4H6Cl3F

Conditions
ConditionsYield
With tris[(2-pyridylmethyl)amine]; copper(l) chloride In N,N-dimethyl-formamide at 130℃; for 14h;15%
HCFC-141b
1717-00-6

HCFC-141b

1,1-Dichlorethanphosphonsaeuredichlorid
55453-81-1

1,1-Dichlorethanphosphonsaeuredichlorid

Conditions
ConditionsYield
With aluminium trichloride; phosphorus trichloride Behandeln des Reaktionsgemisches mit Wasser und Dichlormethan bei -20grad;
HCFC-141b
1717-00-6

HCFC-141b

C2H2Cl2F

C2H2Cl2F

Conditions
ConditionsYield
With hydroxyl Kinetics; flash-photolysis - laser-induced fluorescence;
With hydroxide In gaseous matrix at -23.1 - 23.9℃; under 0.06 - 0.2 Torr; Kinetics;
With hydroxide at 19.9℃; under 37.5 Torr; Rate constant; Thermodynamic data; ΔHR;
With tetrachloromethane at 24.85℃; under 40 Torr; Kinetics; Further Variations:; Temperatures; radical reaction; Photolysis;
HCFC-141b
1717-00-6

HCFC-141b

N-tert-butyl-α-phenylnitrone
3376-24-7

N-tert-butyl-α-phenylnitrone

A

benzoyl-tert-butylnitroxyl radical
35822-90-3

benzoyl-tert-butylnitroxyl radical

B

C11H15ClNO
29271-97-4

C11H15ClNO

C

C13H18ClFNO

C13H18ClFNO

Conditions
ConditionsYield
Irradiation; Title compound not separated from byproducts;
HCFC-141b
1717-00-6

HCFC-141b

A

C2H3ClFO2

C2H3ClFO2

B

C2H2Cl2FO2

C2H2Cl2FO2

Conditions
ConditionsYield
With oxygen at -20.1 - 47.9℃; under 4 - 60 Torr; Kinetics; Mechanism; Irradiation; UV flash photolysis; formation of chloro and peroxyradicals was detected by time-resolved MS;
HCFC-141b
1717-00-6

HCFC-141b

A

2,2,2-trifluoroethanol
420-46-2

2,2,2-trifluoroethanol

B

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

C

1-chloro-1-fluoroethane
2317-91-1

1-chloro-1-fluoroethane

D

1,1-Dichloroethylene
75-35-4

1,1-Dichloroethylene

E

acetic acid
64-19-7

acetic acid

Conditions
ConditionsYield
fluorinated γ-alumina at 300℃; Product distribution; other temperatures; also with HCl or HF as reagents;
HCFC-141b
1717-00-6

HCFC-141b

1-Chloro-1,1-difluoroethane
75-68-3

1-Chloro-1,1-difluoroethane

Conditions
ConditionsYield
With hydrogen fluoride Heating;
HCFC-141b
1717-00-6

HCFC-141b

A

formaldehyd
50-00-0

formaldehyd

B

fluorodichloromethyl
1691-90-3

fluorodichloromethyl

C

dichlorofluoroacetaldehyde
63034-44-6

dichlorofluoroacetaldehyde

D

1,1-Dichloro-1-fluoro-2-nitrosooxy-ethane

1,1-Dichloro-1-fluoro-2-nitrosooxy-ethane

Conditions
ConditionsYield
With oxygen; nitrogen(II) oxide; chlorine at 19.9℃; under 37.5 Torr; Rate constant; Thermodynamic data; Product distribution; Irradiation; ΔHR, var. of ratios;
HCFC-141b
1717-00-6

HCFC-141b

C2H3ClF

C2H3ClF

Conditions
ConditionsYield
With air; hydrogen; ozone at 30℃; under 50 Torr; Rate constant; Irradiation;
HCFC-141b
1717-00-6

HCFC-141b

C2H2Cl2FNO4

C2H2Cl2FNO4

Conditions
ConditionsYield
With oxygen; chlorine; Nitrogen dioxide radical reaction; Photolysis;

1717-00-6Relevant articles and documents

Substituent effects and threshold energies for the unimolecular elimination of HCl (DCl) and HF (DF) from chemically activated CFCl2CH3 and CFCl2CD3

McDoniel, J. Bridget,Holmes, Bert E.

, p. 3044 - 3050 (1996)

Combination of CFCl2 and methyl-d0 and -d3 radicals form CFCl2CH3-d0 and -d3 with 100 and 101 kcal/mol of internal energy, respectively. An upper limit for the rate constant ratio of disproportionation to combination, kd/kc, for Cl transfer is 0.07 ± 0.03 for collision of two CFCl2 radicals and 0.015 ± 0.005 for CH3 and CFCl2 radicals. The chemically activated CFCl2CH3 undergoes 1,2-dehydrochlorination and 1,2-dehydrofluorination with rate constants of 3.9 × 109 and 4.9 × 107 s-1, respectively. For CFCl2CD3 the rate constants are 8.7 × 108 s-1 for loss of DCl and 1.1 × 107 s-1 for DF. The kinetic isotope effect is 4.4 ± 0.9 for HCl/DCl and appears to be identical for HF/DF. Threshold energies are 54 kcal/mol for loss of HCl and 68 kcal/mol for HF; the E0's for the deuterated channels are 1.4 kcal/mol higher. Comparison of these threshold energies with other haloethanes suggests that for HF and HCl elimination the transition states are developing charges of different signs on the carbon containing the departing halogen and that chlorine and fluorine substituents exert similar inductive effects.

Liquid-phase fluorination of 1,1,1-trichloroethane

Brunet, S.,Batiot, C.,Barrault, J.,Blanchard, M.

, p. 33 - 39 (1992)

The reaction of HF with SbCl5 at 60 deg C and 1 MPa provides antimony mixed halides whose empirical formulae have been determined.The product is a mixture of SbClF4 and SbClF2 solvated by HF and its activity has been measured for the conversion of 1,1,1-trichloroethane (F140a) into mono- and difluorochloroethane (F141b and F142b).

Method of making difluoromethane, 1,1,1-trifluoroethane and 1,1-difluoroethane

-

Page/Page column 3, (2010/02/14)

A process for the production of difluoromethane (HFC-32), 1,1,1-trifluoroethane (HFC-143a) and 1,1-difluoroethane (HFC-152a). In the process the following steps are employed: (a) providing a reaction vessel, (b) providing in the reaction vessel activated carbon impregnated with a strong Lewis acid fluorination catalys selected from halides of As, Sb, Al, TI, In, V, Nb, Ta, Ti, Zr and Hf, (c) activating the catalyst by passing through the activated carbon impregnated with a strong Lewis acid fluorination catalyst anhydrous hydrogen fluoride gas and chlorine gas, (d) contacting, in a vapor state in the reaction vessel containing the activated catalyst, hydrogen fluoride and one or more halogenated hydrocarbons selected from chlorofluoromethane, dichloromethane, 1,1,1-trichloroethane, vinyl chloride, 1,1-dichloroethylene, 1.2-dichloroethylene, 1,2-dichloroethane, and 1,1-dichloroethane for a time and at a temperature to produce a product stream comprising hydrofluorocarbon product(s) corresponding to the chlorinated hydrocarbon reactant(s), and one or more of hydrogen chloride, unreactacted chlorinated hydrocarbon reactant(s), under-fluorinated intermediates, and unreacted hydrogen fluoride, and (e) separating the hydrofluorocarbon product(s) from the product stream.

Production of organic fluorine compounds

-

, (2008/06/13)

A process is disclosed for hydrofluorinating an olefinic hydrocarbon of the formula where X, X' and X" are the same or different and are hydrogen or halo and R' is hydrogen or C1 -C6 alkyl, with hydrogen fluoride. The process is carried out by admixing the olefinic hydrocarbon with hydrogen fluoride in an imidofluoride hydrogen fluoride solvent having the formula where R is C1 to C6 alkyl, C1 to C6 alkyl substituted with halo or C6 to C10 aryl either unsubstituted or substituted with alkyl and η is 0 or an integer that is at least 1.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1717-00-6