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ChemicalBook >  Product Catalog >  Organic Chemistry >  Hydrocarbons and derivatives >  Hydrocarbon halides >  2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE

2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE

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2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE Basic information

Product Name:
2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE
Synonyms:
  • 4-(TRIFLUOROMETHYL)-2,3,5,6-TETRAFLUOROBENZYL BROMIDE
  • 4-(TRIFLUOROMETHYL)TETRAFLUOROBENZYL BROMIDE
  • 4-(BROMOMETHYL)-2,3,5,6-TETRAFLUORO-BENZOTRIFLUORIDE
  • 2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE
  • 1-(BROMOMETHYL)-2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZENE
  • TTBB
  • (4-BROMOMETHYL)HEPTAFLUOROTOLUENE
  • 1-(bromomethyl)tetrafluoro-4-(trifluoromethyl)benzene
CAS:
76437-40-6
MF:
C8H2BrF7
MW:
310.99
Mol File:
76437-40-6.mol
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2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE Chemical Properties

Boiling point:
190.0±35.0 °C(Predicted)
Density 
1.864 g/mL at 25 °C (lit.)
vapor pressure 
0.38 psi ( 20 °C)
refractive index 
n20/D 1.448(lit.)
Flash point:
210 °F
form 
liquid
color 
Clear
Sensitive 
Lachrymatory
BRN 
8423469
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
19
Hazard Note 
Harmful/Lachrymatory
HazardClass 
8
PackingGroup 
III
HS Code 
29039990

MSDS

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2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE Usage And Synthesis

Uses

2,3,5,6-Tetrafluoro-4-(trifluoromethyl)benzyl bromide (4-(trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide, TTBB) may be employed as an alternate of pentafluorobenzyl bromide (PFBB) in electrophoric derivatization reactions prior to detection during gas chromatography-electron-capture negative ion mass spectrometry (GC-ECNI-MS). TTBB may be employed as derivatization reagent for the characterization and quantitation of DNA and hemoglobin adducts.

General Description

2,3,5,6-Tetrafluoro-4-(trifluoromethyl)benzyl bromide (4-(trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide) has been reported to be prepared in one step from α,α,α?2,3,5,6-heptafluoro-p-xylene.

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