77342-37-1

Basic information

• Product Name: 5,5,5-TRIFLUOROPENT-1-EN-4-OL
• Synonyms: 5,5,5-TRIFLUOROPENT-1-EN-4-OL;5,5,5-Trifluoropent-1-en-4-ol 97%;5,5,5-Trifluoropent-1-en-4-ol97%;1,1,1-Trifluoropent-4-en-2-ol 97%;5,5,5-Trifluoropent-1-en-4-ol, 4-Hydroxy-5,5,5-trifluoropent-1-ene;1,1,1-Trifluoropent-4-en-2-ol97%
• CAS NO: 77342-37-1
• Molecular Formula: C₅H₇F₃O
• Molecular Weight: 140.1
• Mol File: 77342-37-1.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 100-101
• Flash Point: 56.81°C
• Appearance: /
• Density: 1.163g/cm³
• Vapor Pressure: 12.675mmHg at 25°C
• Refractive Index: 1.365
• PKA: 12.33±0.20(Predicted)
• CAS DataBase Reference: 5,5,5-TRIFLUOROPENT-1-EN-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5,5-TRIFLUOROPENT-1-EN-4-OL(77342-37-1)
• EPA Substance Registry System: 5,5,5-TRIFLUOROPENT-1-EN-4-OL(77342-37-1)

Safety Data

• Hazard Codes: F
• Hazardous Substances Data: 77342-37-1(Hazardous Substances Data)

Usage

General Description

5,5,5-Trifluoropent-1-en-4-ol, also known as trifluoropentenol, is a fluorinated organic compound with the molecular formula C5H6F3OH. It is a colorless liquid at room temperature and is used as a building block in organic synthesis to produce pharmaceuticals, agrochemicals, and other fine chemicals. Trifluoropentenol is a versatile intermediate in the synthesis of complex organic molecules due to its functional group, which allows for further chemical manipulation. It is also used as a reagent in various chemical reactions, such as the addition of nucleophiles and organometallic reagents, making it an important compound in the field of organic chemistry. Additionally, trifluoropentenol has potential applications in the development of new materials and as a building block for fluorine-containing polymers. Overall, 5,5,5-trifluoropent-1-en-4-ol is a valuable chemical with diverse uses in the chemical industry.

InChI:InChI=1/C5H7F3O/c1-2-3-4(9)5(6,7)8/h2,4,9H,1,3H2

Upstream product

• 383-63-1 ethyl trifluoroacetate, 
• 24850-33-7 allyltributylstanane 
• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 106-95-6 allyl bromide 
• 762-72-1 allyl-trimethyl-silane 
• 433-27-2 ethyl trifluoroacetaldehyde hemiacetal 
• 421-53-4 2,2,2-trifluoro-1,1-ethanediol 
• 1730-25-2 allylmagnesium bromide 
• 431-46-9 2,2,2-trifluoro-1-methoxy-ethanol 

Relevant articles and documents

A versatile and practical synthesis of α-trifluoromethylated alcohols from trifluoroacetaldehyde ethyl hemiacetal in water

α-Trifluoromethylated alcohols via indium-mediated allylation of trifluoroacetaldehyde using a simple and practical preparation in water is described.

Towards the syntheses of α-trifluoromethylated oxygenated heterocycles and their precursors

The possibilities of synthesizing various α-trifluoro-methylated oxygenated heterocycles, starting from trifluoroacetaldehyde methyl hemiacetal, through classic cyclization reactions, have been demonstrated. In this way, six-membered cyclic compounds, δ-l

1,8-bis(allylstannyl)naphthalene derivatives as neutral allylation agents: Rate acceleration by chelation-induced Lewis acidity

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