1-bromoperfluorohexane
Names
[ CAS No. ]:
335-56-8
[ Name ]:
1-bromoperfluorohexane
[Synonym ]:
Tridecafluorohexyl Bromide
n-1-bromoperfluorohexane
EINECS 206-391-6
MFCD00042349
1-Bromoperfluorohexane
1-Bromotridecafluorohexane
Perfluorohexyl bromide
bromotridecafluorohexane
Chemical & Physical Properties
[ Density]:
1.871 g/mL at 25 °C(lit.)
[ Boiling Point ]:
97 °C(lit.)
[ Melting Point ]:
-49ºC
[ Molecular Formula ]:
C6BrF13
[ Molecular Weight ]:
398.94700
[ Flash Point ]:
100-101°C
[ Exact Mass ]:
397.89800
[ LogP ]:
5.07760
[ Index of Refraction ]:
n20/D 1.3(lit.)
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
[ Hazard Codes ]:
Xi: Irritant;
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2903799090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2903799090
[ Summary ]:
2903799090 halogenated derivatives of acyclic hydrocarbons containing two or more different halogens。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%
Articles
Am. J. Physiol. Lung Cell. Mol. Physiol. 278(5) , L1018-24, (2000)
Preclinical studies comparing perflubron partial liquid ventilation with conventional mechanical ventilation have indicated that perflubron partial liquid ventilation may exert some anti-inflammatory ...
A general synthesis of fluoroalkylated alkenes by palladium-catalyzed Heck-type reaction of fluoroalkyl bromides.Angew. Chem. Int. Ed. Engl. 54(4) , 1270-4, (2015)
An efficient palladium-catalyzed Heck-type reaction of fluoroalkyl halides, including perfluoroalkyl bromides, trifluoromethyl iodides, and difluoroalkyl bromides, has been developed. The reaction pro...
Triphenylsilyl as a protecting group in the synthesis of 1, 12-heterodisubstituted p-carboranesJ. Org. Chem. 65(5) , 1434-41, (2000)
A triphenylsilyl group is used as an auxiliary in the synthesis of heterodisubstituted p-carboranes via triphenylsilyl-p-carborane (1). The preparation of 1 is statistical, but with recovery of the st...