378-34-7

Basic information

• Product Name: HEPTAFLUOROISOPROPYLBENZENE 98
• Synonyms: HEPTAFLUOROISOPROPYLBENZENE 98;Heptafluoroisopropylbenzene 98%;[1,2,2,2-Tetrafluoro-1-(trifluoromethyl)ethyl]benzene;7,8,8,8,9,9,9-Heptafluorocumene
• CAS NO: 378-34-7
• Molecular Formula: C₉H₅F₇
• Molecular Weight: 246.1245
• Mol File: 378-34-7.mol
• Article Data: 6

Chemical Properties

• Melting Point: -10
• Boiling Point: 127-128
• Flash Point: 28.5°C
• Appearance: /
• Density: 1.488
• Vapor Pressure: 20.7mmHg at 25°C
• Refractive Index: 1.411
• CAS DataBase Reference: HEPTAFLUOROISOPROPYLBENZENE 98(CAS DataBase Reference)
• NIST Chemistry Reference: HEPTAFLUOROISOPROPYLBENZENE 98(378-34-7)
• EPA Substance Registry System: HEPTAFLUOROISOPROPYLBENZENE 98(378-34-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 378-34-7(Hazardous Substances Data)

Usage

General Description

HEPTAFLUOROISOPROPYLBENZENE 98 is a fluorocarbon compound with a purity of 98%. It is a clear, colorless liquid with a sharp, slightly sweet odor. This chemical is commonly used as a solvent in various industrial applications, including the manufacturing of electronic components, specialty polymers, and chemical synthesis. HEPTAFLUOROISOPROPYLBENZENE 98 is also known for its low toxicity and high chemical stability, making it suitable for use in controlled environments. Additionally, its unique properties, such as high thermal stability and electrical resistance, make it a valuable component in the production of advanced materials and electronic devices.

InChI:InChI=1/C9H5F7/c10-7(8(11,12)13,9(14,15)16)6-4-2-1-3-5-6/h1-5H

Upstream product

• 677-69-0 perfluoroisopropyl iodide 
• 71-43-2 benzene 
• 98-80-6 phenylboronic acid 
• 116-15-4 perfluoropropylene 
• 718-64-9 1,1,1,3,3,3-hexafluoro-2-phenylisopropyl alcohol 
• 591-50-4 iodobenzene 

Downstream Products

• 1979-51-7 1,1,3,3,3-pentafluoro-2-phenylpropene 
• 3142-78-7 1,1,1,3,3,3-hexafluoro-2-phenylpropane 
• 2396-18-1 m-(Heptafluorisopropyl)-N,N-dimethylanilin 
• 2396-16-9 3-iso-C₃F₇C₆H₄NH₂ 
• 2396-20-5 m-(Heptafluorisopropyl)-benzoesaeure 
• 2396-24-9 m-Fluor-(heptafluorisopropyl)-benzol 
• 2396-22-7 1-bromo-3-heptafluoroisopropylbenzene 
• 2396-13-6 1-nitro-3-(perfluoropropan-2-yl)benzene 
• 2021-68-3 perfluoroisopropylcyclohexane 

Relevant articles and documents

METHOD FOR PREPARATION OF FLUORO ALKYLATED COMPOUNDS BY HOMOGENEOUS NI CATALYSIS

The invention discloses a method for the preparation of fluoro alkylated compounds by homogeneous Ni catalyzed fluoro alkylation with fluoro alkyl halides in the presence of a base.

Direct heptafluoroisopropylation of arylboronic acids via hexafluoropropene (HFP)

A novel and straightforward strategy for heptafluoroisopropylation of arylboronic acids at room temperature has been developed. This method, directly using commercial available hexafluoropropene (HFP) as the starting material, provides a new way to synthesize a variety of synthetically useful heptafluoroisopropylated arenes.

Syntheses of lipophilic tetraarylborate ions substituted with many perfluoroalkyl groups and their stability under acid conditions

Syntheses are investigated on several new kinds of perfluoroalkyl-substituted tetraarylborate ions such as tetrakis(3,5-bis(nonafluorobutyl)phenyl)borate, tetrakis(3,5-bis(heptafluoro-2-propyl)phenyl)borate (PFPB), tetrakis(3-(heptafluoro-2-propyl)-1-(tri