| Identification | More | [Name]
GERANYL BROMIDE | [CAS]
6138-90-5 | [Synonyms]
1-BROMO-3,7-DIMETHYL-2,6-OCTADIENE
GERANYL BROMIDE
TRANS-1-BROMO-3,7-DIMETHYL-2,6-OCTADIENE
(2E)-1-Bromo-3,7-dimethyl-2,6-octadiene
7-dimethyl-6-octadien(e)-1-bromo-3
(E)-1-bromo-3,7-dimethylocta-2,6-diene
Geranylbromide,97%
(2E)-1-Bromo-3,7-dimethyl-2,6-octadienine
(6E)-2,6-Dimethyl-8-bromo-2,6-octadiene
(E)-3,7-Dimethyl-2,6-octadienyl bromide
[(2E)-3,7-Dimethyl-2,6-octadienyl] bromide | [EINECS(EC#)]
228-123-7 | [Molecular Formula]
C10H17Br | [MDL Number]
MFCD00000243 | [Molecular Weight]
217.15 | [MOL File]
6138-90-5.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
2810 | [WGK Germany ]
3
| [F ]
8-10-19 | [TSCA ]
Yes | [HazardClass ]
6.1(b) | [PackingGroup ]
III |
| Hazard Information | Back Directory | [Uses]
Geranyl bromide is used for the preparation of 3,7-dihydroxyflavone derivatives and baicalein. It is also involved in the synthesis of potential flavonoidic modulators of P-glycoprotein activity. Further, it reacts with benzenesulfinic acid to prepare geranyl phenyl sulfone. In addition to this, it takes part in the palladium catalyzed cross coupling with aryl and alkenylgold(I) phosphanes. | [General Description]
Geranyl bromide undergoes palladium catalyzed cross-coupling reaction with aryl and alkenylgold(I) phosphanes. |
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