| Identification | More | [Name]
2,6-Difluorobenzyl bromide | [CAS]
85118-00-9 | [Synonyms]
2,6-DIFLUOROBENZYL BROMIDE
2-BROMOMETHYL-1,3-DIFLUORO-BENZENE
ALPHA-BROMO-2,6-DIFLUOROTOLUENE
TIMTEC-BB SBB006564
Benzene, 2-(bromomethyl)-1,3-difluoro-
à-bromo-2,6-difluorotoluene
α-bromo-2,6-difluorotoluene
2,6-Difluorobenzyl bromide 98%
2,6-Difluorobenzylbromide98%
2，6-Diflurobenzylbromide
A-BROMO-2,6-DIFLUOROTOLUENE
2,6-DIFLUORO BENZYL BROMOIDE
2,6-Difluorobenzyl bromide, 97+%
1-(Bromomethyl)-2,6-difluorobenzene
1,3-Difluoro-2-(bromomethyl)benzene | [EINECS(EC#)]
285-652-6 | [Molecular Formula]
C7H5BrF2 | [MDL Number]
MFCD00000329 | [Molecular Weight]
207.02 | [MOL File]
85118-00-9.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
52-55 °C(lit.)
| [Boiling point ]
184.9±25.0 °C(Predicted) | [density ]
1,6 g/cm3 | [refractive index ]
1.5256 (estimate) | [Fp ]
>230 °F
| [storage temp. ]
Inert atmosphere,2-8°C | [form ]
Crystalline Powder | [color ]
Almost white to light beige | [Sensitive ]
Lachrymatory | [BRN ]
2083943 | [InChIKey]
LSXJPJGBWSZHTM-UHFFFAOYSA-N | [CAS DataBase Reference]
85118-00-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns.
R36:Irritating to the eyes. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S25:Avoid contact with eyes .
S27:Take off immediately all contaminated clothing . | [RIDADR ]
UN 3261 8/PG 2
| [WGK Germany ]
3
| [F ]
10-19-21 | [Hazard Note ]
Corrosive/Lachrymatory | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29039990 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
2,6-Difluorobenzyl bromide has been used:
- as reagent in alkylation of the quinazoline-2-thioxo-4-one
- in the synthesis of 1,3,5-triazine-2,4,6-triones
- in the preparation of new classes of inhibitors of bovine viral diarrhea virus (as a surrogate virus for hepatitis C virus)
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