383-68-6

Basic information

• Product Name: 1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate
• Synonyms: 1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate;2-BROMO-3,3,3-TRIFLUOROPROPYL ACETATE, 98% MIN.;2-BROMO-3,3,3-TRIFLUOROPROPYL ACETATE;2-Bromo-3,3,3-trifluoro-1-propanol acetate;3-Acetoxy-2-bromo-1,1,1-trifluoropropane
• CAS NO: 383-68-6
• Molecular Formula: C₅H₆BrF₃O₂
• Molecular Weight: 235.01
• Mol File: 383-68-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 151.9°C at 760 mmHg
• Flash Point: 45.7°C
• Appearance: /
• Density: 1.626g/cm³
• Vapor Pressure: 3.59mmHg at 25°C
• Refractive Index: 1.401
• CAS DataBase Reference: 1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate(383-68-6)
• EPA Substance Registry System: 1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate(383-68-6)

Safety Data

• Hazardous Substances Data: 383-68-6(Hazardous Substances Data)

Usage

General Description

1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate is a chemical compound with the formula C6H9BrF3O2. It is an organic compound that is often used as a solvent in various industries. 1-Propanol, 2-bromo-3,3,3-trifluoro-, acetate is derived from 1-propanol and is modified with the addition of bromine and trifluoromethyl groups, resulting in an acetate compound that is commonly used in chemical research and manufacturing processes. It is valued for its ability to dissolve various substances and its application in organic synthesis and as a reaction solvent. Additionally, it is known for its high stability and low toxicity, making it a desirable compound for a variety of industrial applications.

InChI:InChI=1/C5H6BrF3O2/c1-3(10)11-2-4(6)5(7,8)9/h4H,2H2,1H3

Upstream product

• 677-21-4 1,1,1-trifluoropropylene 
• 64-19-7 acetic acid 
• 563-85-9 1,1,2-trifluoropropene 

Downstream Products

• 1514-82-5 2-bromo-3,3,3-trifluoropropene 
• 311-86-4 2-bromo-3,3,3-trifluoropropan-1-ol 
• 64-19-7 acetic acid 
• 359-41-1 1,1,1-trifluoro-2,3-epoxypropane 

Relevant articles and documents

Preparation method of 3,3,3-trifluoropropylene carbonate

The invention discloses a preparation method of 3,3,3-trifluoropropylene carbonate. The preparation method comprises the steps: with trifluoropropylene as a raw material, carrying out several simple reaction steps to obtain trifluoroepoxy propane, introducing carbon dioxide into a high-pressure reaction kettle by taking a metal conjugated microporous polymer complex as a catalyst, and preparing 3,3,3-trifluoropropylene carbonate at the temperature of 25-100 DEG C and the pressure of 0.1Mpa-3Mpa. Compared with the prior art, the method has the advantages that trifluoropropylene is taken as theraw material, so that the raw material cost is substantially lowered; and meanwhile, the yield is relatively high, and the catalyst can be repeatedly used, so that the method is suitable for industrial production.

Methods for preparing Halohydrins and methods for preparing Epoxides

The invention includes methods for preparing halohydrins and epoxides. A method of preparing halohydrins can include exposing (R1CHXCH2O—)2SO2 to R2COOH to produce R1CHXCH2COOR2 and hydrolyzing the R1CHXCH2COOR2 to produce the halohydrin R1CHXCH2OH. R1 and R2 can be the same or different single elements and/or organic groups and X can be a halogen. A method of preparing an epoxide can include combining a sulfuric acid containing solution with a halogen to produce a first mixture and exposing the first mixture to trifluoropropene to produce a second mixture. The second mixture can be combined with acetic acid to produce an acetyl halohydrin of trifluoropropene and the acetyl halohydrin can be hydrolyzed to form a halohydrin of trifluoropropene. The halohydrin can be converted to a trifluoropropyl epoxide.