116586-94-8

Basic information

• Product Name: 3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL
• Synonyms: 3,3-DIMETHOXY-1,1,1-TRIFLUOROPROPANE;3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL;3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL, 97% MIN.;3,3,3-Trifluoropropanaldimethylacetal97%
• CAS NO: 116586-94-8
• Molecular Formula: C₅H₉F₃O₂
• Molecular Weight: 158.12
• Mol File: 116586-94-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 62.8°Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.124g/cm³
• Vapor Pressure: 188mmHg at 25°C
• Refractive Index: 1.335
• CAS DataBase Reference: 3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL(116586-94-8)
• EPA Substance Registry System: 3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL(116586-94-8)

Safety Data

• Hazard Codes: F
• HazardClass: FLAMMABLE
• Hazardous Substances Data: 116586-94-8(Hazardous Substances Data)

Usage

General Description

3,3,3-Trifluoropropanal dimethylacetal is a chemical compound with the molecular formula C5H8F6O. It is a colorless liquid and is commonly used as a solvent in various chemical processes. 3,3,3-TRIFLUOROPROPANAL DIMETHYLACETAL is also known for its strong and sweet odor, making it suitable for use in perfumes and other fragrances. Additionally, 3,3,3-Trifluoropropanal dimethylacetal has been used in the synthesis of pharmaceuticals and other organic compounds. Its unique chemical properties and versatility make it a valuable ingredient in various industrial applications.

InChI:InChI=1/C5H9F3O2/c1-9-4(10-2)3-5(6,7)8/h4H,3H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 26885-67-6 (Z)-1-Methoxy-3,3,3-trifluoroprop-1-ene 
• 26885-67-6 E/Z-1-methoxy-3,3,3-trifluoropropene 
• 754-12-1 2,3,3,3-tetrafluoro-propene 
• 677-21-4 1,1,1-trifluoropropylene 

Downstream Products

• 2516-99-6 3,3,3-Trifluoropropionic acid 
• 18830-44-9 methyl 3,3,3-trifluoropropionate 
• 460-40-2 3,3,3-trifluoropropanal 

Relevant articles and documents

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.

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.

Convenient synthesis of 3,3,3-trifluoropropanoic acid by hydrolytic oxidation of 3,3,3-trifluoropropanal dimethyl acetal

A convenient and efficient method for preparing 3,3,3-trifluoropropanoic acid (1) is reported. The starting material is 1-chloro-3,3,3-trifluoropropene (2) that can be easily transformed into 3,3,3-trifluoropropanal dimethyl acetal (4) on treatment with methanol and KOH followed by acid-catalyzed addition of methanol. Direct transformation of 4 into 1 was efficiently achieved with 30% aqueous hydrogen peroxide (4.0 equiv.) in the presence of FeCl3 (0.025 equiv.) and hydrochloric acid (0.5 equiv.).