688-29-9

Basic information

• Product Name: 3,3-diethoxy-1,1,1-trifluoropropane
• CAS NO: 688-29-9
• Molecular Formula: C₇H₁₃F₃O₂
• Molecular Weight: 186.1721
• Mol File: 688-29-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 117.6°C at 760 mmHg
• Flash Point: 30.5°C
• Density: 1.072g/cm³
• Vapor Pressure: 20.6mmHg at 25°C
• Refractive Index: 1.36
• CAS DataBase Reference: 3,3-diethoxy-1,1,1-trifluoropropane(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-diethoxy-1,1,1-trifluoropropane(688-29-9)
• EPA Substance Registry System: 3,3-diethoxy-1,1,1-trifluoropropane(688-29-9)

Safety Data

• Hazardous Substances Data: 688-29-9(Hazardous Substances Data)

Usage

General Description

3,3-diethoxy-1,1,1-trifluoropropane is a chemical compound with the molecular formula C7H13F3O2. It is a colorless liquid with a characteristic odor, and it is primarily used as a solvent in various industrial applications. It is also used as a reagent in organic synthesis and as a propellant in aerosol products. The compound is flammable and should be handled with caution, as it can pose a risk of fire or explosion. In addition, it may have harmful effects if inhaled, ingested, or in contact with skin, and proper safety measures should be taken when working with this chemical.

Upstream product

• 64-17-5 ethanol 
• 122372-43-4 2-(2,2,2-trifluoroethyl)-1,3-dithiane 
• 126015-38-1 1-ethoxy-3,3,3-trifluoro-1-propene 
• 126015-28-9 (Z)-1-ethoxy-3,3,3-trifluoroprop-1-ene 
• 754-12-1 2,3,3,3-tetrafluoro-propene 
• 677-21-4 1,1,1-trifluoropropylene 

Downstream Products

• 201861-97-4 1,1-Bisbenzylthio-3,3,3-trifluoropropane 
• 460-40-2 3,3,3-trifluoropropanal 

Relevant articles and documents

Atom-economical synthesis of 3,3,3-trifluoropropanal dialkyl acetals through Pd/C catalyzed acetalization of 3,3,3-trifluoropropene

A facile and efficient procedure for one-step synthesis of 3,3,3-trifluoropropanal dialkyl acetals from readily available 3,3,3-trifluoropropene (TFP) has been developed. The catalyst can be recycled for 4 times without obvious deactivation. This process provides a novel and atom-economical synthetic strategy for the preparation of functional CF3-containing compounds.

A novel and convenient synthesis of (Z)-3,3,3-trifluoropropenyl alkyl ethers and CF3-substituted propyl acetals as versatile CF3-containing building blocks

A novel and convenient preparation of (Z)-3,3,3-trifluoropropyl alkyl ethers and their further transformation into CF3-substituted propyl acetals is described.

β-PERFLUOROALKYLVINYL ALKYL ETHERS

A convenient method was developed for the synthesis of β-perfluoroalkyl-substituted vinyl ethers by the reaction of vinyl alkyl ethers with perfluoroalkyl iodides in the presence of a palladium catalyst.Fluorine-containing aldehydes and their acetals, in which the perfluoroalkyl radical is separated from the formyl group by a methylene unit, were synthesized from the ethers.These aldehydes can be used for the synthesis of β-perfluoroalkyldicarbocyanines.