52067-19-3

Basic information

• Product Name: 1-fluoroethyl
• Synonyms: Ethyl, 1-fluoro-
• CAS NO: 52067-19-3
• Molecular Formula: C₂H₄F
• Molecular Weight: 47.0516
• Mol File: 52067-19-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-fluoroethyl(CAS DataBase Reference)
• NIST Chemistry Reference: 1-fluoroethyl(52067-19-3)
• EPA Substance Registry System: 1-fluoroethyl(52067-19-3)

Safety Data

• Hazardous Substances Data: 52067-19-3(Hazardous Substances Data)

Usage

Physical state

Colorless gas at room temperature

Flammability

Flammable

Uses

a. Intermediate in the production of pharmaceuticals
b. Intermediate in the production of agricultural chemicals
c. Production of fluorinated polymers
d. Starting material in the synthesis of other organic compounds

Toxicity

Toxic and hazardous material

Safety precautions

Proper safety precautions should be taken when handling and storing

Environmental and health regulations

Use is regulated in many countries to prevent environmental contamination and adverse health effects

Upstream product

• 353-36-6 1-fluoroethane 

Relevant articles and documents

Reactions of ground state chlorine atoms with fluorinated methanes and ethanes

The reactions of photochemically generated Cl(2Pj) atoms with a number of fluorohydrocarbons have been investigated in the temperature range 8-95 deg C by the competitive photochlorination technique using CH4 as a primary standard.Relative and absolute rate parameters are reported for CH3F, CH2F2, CH3CH2F, CH2FCH2F, CH3CHF2, CH3CF3, CH2FCHF2, CHF2CHF2, and several auxiliary reactions including CH3Cl, C2H6, and C3H8.The internal competition for hydrogen abstraction in asymmetric fluorethanes is examined in detail.The reactivity trends are discussed and it is found that the activation energies in the fluoromethane series correlate with the known C-H bond dissociation energies.The hydrogen reactivity in the fluoroethane series for which a sufficient data base of DH(C-H) values is not available is best rationalized in terms of inductive effects and resonance interactions.