3925-78-8

Basic information

• Product Name: 1,2,3-TRIBROMO-5-FLUOROBENZENE, 99+%
• Synonyms: 1,2,3-TRIBROMO-5-FLUOROBENZENE, 99+%
• CAS NO: 3925-78-8
• Molecular Formula: C₆H₂Br₃F
• Molecular Weight: 332.7904832
• Mol File: 3925-78-8.mol
• Article Data: 2

Chemical Properties

• Melting Point: 98 °C
• Boiling Point: 260.9±35.0 °C(Predicted)
• Appearance: /
• Density: 2.3899 (rough estimate)
• Refractive Index: 1.4640 (estimate)
• CAS DataBase Reference: 1,2,3-TRIBROMO-5-FLUOROBENZENE, 99+%(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3-TRIBROMO-5-FLUOROBENZENE, 99+%(3925-78-8)
• EPA Substance Registry System: 1,2,3-TRIBROMO-5-FLUOROBENZENE, 99+%(3925-78-8)

Safety Data

• Hazardous Substances Data: 3925-78-8(Hazardous Substances Data)

Usage

Chemical Properties

PINK TO BROWNISH SHINY SMALL NEEDLES

Upstream product

• 462-06-6 fluorobenzene 
• 147-82-0 2,4,6-tribromoaniline 

Downstream Products

• 576-85-2 1,3,5-trideutero-2-fluorobenzene 

Relevant articles and documents

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PHOTOCHEMICAL BROMINATION OF ARENES. 2. FLUOROBENZENE DERIVATIVES (1)

Photochemically induced reaction of fluorobenzene and a range of polyfluorobenzenes, both in an excess of the arene and with fluorotrichloromethane as solvent, gave isolable adducts only with fluorobenzene, the isomeric difluorobenzenes, and in very small yield with 1,3,5-trifluorobenzene.These adducts were identified by combustion analysis, mass spectrometry, and n.m.r. techniques (1H, 13C, 19F).In every case, the expected substitution products accompanied these adducts, and in the more fully fluorinated benzene derivatives substitution was the only process observed.Fluorotrichloromethane encouraged the formation of adducts, but the concurrent formation of substantial amounts of substitution products suggested that adducts are not the necessary precursors of the substitution products, in contrast with other systems.