97168-13-3

Basic information

• Product Name: 1,1,2-TRIFLUOROBUT-1-EN-4-OL
• Synonyms: 1,1,2-TRIFLUOROBUT-1-EN-4-OL;1,1,2-Trifluorobut-1-en-4-ol 97%;1,1,2-Trifluorobut-1-en-4-ol97%;1,1,2-Trifluorobut-1-en-4-ol, 4-Hydroxy-1,1,2-trifluorobut-1-ene;3,4,4-Trifluorobut-3-en-1-ol 97%;3,4,4-Trifluorobut-3-en-1-ol97%
• CAS NO: 97168-13-3
• Molecular Formula: C₄H₅F₃O
• Molecular Weight: 126.08
• Mol File: 97168-13-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 93
• Flash Point: 49.2°C
• Appearance: /
• Density: 1.24g/cm³
• Vapor Pressure: 10.059mmHg at 25°C
• Refractive Index: 1.359
• PKA: 14.37±0.10(Predicted)
• CAS DataBase Reference: 1,1,2-TRIFLUOROBUT-1-EN-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2-TRIFLUOROBUT-1-EN-4-OL(97168-13-3)
• EPA Substance Registry System: 1,1,2-TRIFLUOROBUT-1-EN-4-OL(97168-13-3)

Safety Data

• Hazard Codes: F
• Hazardous Substances Data: 97168-13-3(Hazardous Substances Data)

Usage

General Description

1,1,2-Trifluorobut-1-en-4-ol is a chemical compound with the molecular formula C4H5F3O. It is a colorless liquid with a pungent odor, and it is primarily used as a building block in the synthesis of pharmaceuticals and agrochemicals. 1,1,2-TRIFLUOROBUT-1-EN-4-OL is also used as an intermediate in the production of other organic compounds, such as flavors and fragrances. It is important to handle 1,1,2-Trifluorobut-1-en-4-ol with caution, as it is flammable and may cause irritation to the skin, eyes, and respiratory system. Overall, it is a versatile compound with numerous industrial applications.

InChI:InChI=1/C4H5F3O/c5-3(1-2-8)4(6)7/h8H,1-2H2

Upstream product

• 72469-19-3 (3,4,4-trifluoro-3-butenyl) acetate 
• 145343-35-7 C₁₂H₁₁F₃O₂ 

Downstream Products

• 1418030-75-7 3-((3,4,4-trifluorobut-3-en-1-yl)oxy)cyclohex-2-en-1-one 

Relevant articles and documents

Synthesis of fluorinated tricyclic scaffolds by intramolecular [2+2] photocycloaddition reactions

Fabulous Fluorine: The synthesis of fluorinated products 1 and 2 by [2+2] photocycloaddition was readily feasible after optimization of the irradiation conditions. The electron-deficient trifluoroolefin unit reacted intramolecularly to products 1 (nine ex

Fluorine-contained photoacid generators (PAGs) and corresponding polymer resists

A new series of fluorinated anionic photoacid generators (PAGs) (F4-MBS-TPS, F4VBzBS-TPS, F4-IBBS-TPS, CF3 MBS-TPS, MTFBS-TPS and VBzTFBS-TPS), and corresponding PAG bound polymeric resists (HS-EA-PAG) based on hydroxystyrene (HOST) and 2-ethyl-2-adamanty