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ChemicalBook--->CAS DataBase List--->76437-40-6

76437-40-6

76437-40-6 Structure

76437-40-6 Structure
IdentificationBack Directory
[Name]

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

76437-40-6
[Synonyms]

TTBB
(4-BROMOMETHYL)HEPTAFLUOROTOLUENE
4-(TRIFLUOROMETHYL)TETRAFLUOROBENZYL BROMIDE
4-(BROMOMETHYL)-2,3,5,6-TETRAFLUORO-BENZOTRIFLUORIDE
2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE
1-(bromomethyl)tetrafluoro-4-(trifluoromethyl)benzene
4-(TRIFLUOROMETHYL)-2,3,5,6-TETRAFLUOROBENZYL BROMIDE
1-(BROMOMETHYL)-2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZENE
Benzene, 1-(bromomethyl)-2,3,5,6-tetrafluoro-4-(trifluoromethyl)-
1-(Bromomethyl)-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene, 4-(Trifluoromethyl)-2,3,5,6-tetrafluorobenzyl bromide
[Molecular Formula]

C8H2BrF7
[MDL Number]

MFCD00191855
[MOL File]

76437-40-6.mol
[Molecular Weight]

310.99
Chemical PropertiesBack Directory
[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.)
[Fp ]

210 °F
[form ]

liquid
[color ]

Clear
[Sensitive ]

Lachrymatory
[BRN ]

8423469
Safety DataBack Directory
[Hazard Codes ]

C,Xi
[Risk Statements ]

34
[Safety Statements ]

26-36/37/39-45
[RIDADR ]

UN 3265 8/PG 2
[WGK Germany ]

3
[F ]

19
[Hazard Note ]

Harmful/Lachrymatory
[HazardClass ]

8
[PackingGroup ]

III
[HS Code ]

29039990
Hazard InformationBack Directory
[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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