1-Chloro-1-fluoroethylene

Base Information

• Chemical Name: 1-Chloro-1-fluoroethylene
• CAS No.: 2317-91-1
• Molecular Formula: C2H2ClF
• Molecular Weight: 80.4893
• Hs Code.: 2903799090
• European Community (EC) Number: 219-027-6
• DSSTox Substance ID: DTXSID5073290
• Nikkaji Number: J7.870K
• Wikidata: Q9545650
• Mol file: 2317-91-1.mol

Synonyms:1-chloro-1-fluoroethene

Chemical Property of 1-Chloro-1-fluoroethylene

Chemical Property:

• Appearance/Colour: colourless gas
• Vapor Pressure: 3720mmHg at 25°C
• Melting Point: -169°C
• Refractive Index: 1.353
• Boiling Point: -24°C
• PSA: 0.00000
• Density: 1.098 g/cm³
• LogP: 1.66590
• XLogP3: 1.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 79.9829059
• Heavy Atom Count: 4
• Complexity: 33

Purity/Quality:

98%,99%, ^*data from raw suppliers

1-Chloro-1-fluoroethylene 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F
• Hazard Codes: F
• Statements: 11
• Safety Statements: 9-16-23

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Halogenated Aliphatics, Unsaturated
• Canonical SMILES: C=C(F)Cl

Technology Process of 1-Chloro-1-fluoroethylene

There total 19 articles about 1-Chloro-1-fluoroethylene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

1,2-dichloro-1-fluoroethane (430-57-9) → cis-1,2-Dichloroethylene (156-59-2,43695-79-0) + cis-1-Chloro-2-fluoroethylene (2268-31-7) + trans-1-chloro-2-fluoroethylene (2268-32-8) + fluoroethyne (2713-09-9) + chloroacetylene (593-63-5) + 1-chloro-1-fluoroethane (2317-91-1)

Guidance literature:

under 30 Torr; Product distribution; Thermodynamic data; Mechanism; Irradiation; heats of reaction, influence of pressure, additive gas pressure, pulse number, pulse energy and pulse duration;

DOI:10.1246/bcsj.58.1239

Reference yield:

1,2-dichloro-1-fluoroethane (430-57-9) → cis-1-Chloro-2-fluoroethylene (2268-31-7) + trans-1-chloro-2-fluoroethylene (2268-32-8) + fluoroethyne (2713-09-9) + chloroacetylene (593-63-5) + 1-chloro-1-fluoroethane (2317-91-1) + acetylene (74-86-2,25067-58-7)

Guidance literature:

Mechanism; Irradiation;

DOI:10.1021/j100412a038

Reference yield:

1,2-dichlorofluoroethylene (13245-54-0) → dichloroethyne (7572-29-4) + cis-1-Chloro-2-fluoroethylene (2268-31-7) + fluoroethyne (2713-09-9) + chloroacetylene (593-63-5) + 1-chloro-1-fluoroethane (2317-91-1) + acetylene (74-86-2,25067-58-7)

Guidance literature:

Product distribution; infrared multiphoton decomposition;

DOI:10.1021/j100253a013

upstream raw materials:

1-Chloro-1,1-difluoroethane

1,1,2-trichloro-1-fluoroethane

1-bromo-2,2-dichloro-2-fluoroethane

1,2-dichloro-1-fluoroethane

Downstream raw materials:

2,2,2-trifluoroethanol

1-Chloro-1,1-difluoroethane

Vinylidene fluoride

acetic acid

Refernces

• 1、 Huybrechts,Eerdekens. "Pyrolysis of 1,1-dichloro-1-fluoroethane in the absence and presence of added propene or CCl4: A computer-aided kinetic study". . p. 191 - 197. Retrieved 2001.
• 2、 York, Steven C.,Cox, David F.. "Dehalogenation of 1,1,2-trichloro-1-fluoroethane over ?±-Cr2O3 (101ì?12)". . p. 5182 - 5189. Retrieved 2003.
• 3、 -. "Method for producing fluorine-containing olefin". Paragraph 0348; 0349; 0350; 0351; 0352; 0353. . Retrieved 2017/01/17.