443689
3-Bromo-1,1,1-trifluoropropane
98%
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About This Item
Fórmula lineal:
BrCH2CH2CF3
Número de CAS:
Peso molecular:
176.96
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
assay
98%
refractive index
n20/D 1.363 (lit.)
bp
63.5 °C (lit.)
density
1.662 g/mL at 25 °C (lit.)
SMILES string
FC(F)(F)CCBr
General description
3-Bromo-1,1,1-trifluoropropane is a halogenated hydrocarbon.
Application
3-Bromo-1,1,1-trifluoropropane may be used for the synthesis of 3-(benzyloxy)-N-3,3,3-trifluoropropyl-16,17-seco-estra-1,3,5(10)-triene-16,17-imide and [N-hydroxy-N-(1-trifluoromethylethenyl)]amido
diethylphosphate.
diethylphosphate.
Please view www.aldrich.com/epaods regarding the EPA′s request for application information of Ozone Depleting Substances
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Ozone 1 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves
Certificados de análisis (COA)
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Archives of biochemistry and biophysics, 263(1), 178-190 (1988-05-15)
Leukotriene B4 is rapidly metabolized through omega-oxidation, preventing its detection when it is produced under certain biological conditions. To investigate leukotriene B4 production in various physiological conditions, analogs of arachidonic acid which are converted to metabolically stable analogs of leukotriene
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Molecular cancer therapeutics, 7(8), 2435-2444 (2008-08-30)
An improved steroid sulfatase inhibitor was prepared by replacing the N-propyl group of the second-generation steroid-like inhibitor (2) with a N-3,3,3-trifluoropropyl group to give (10). This compound is 5-fold more potent in vitro, completely inhibits rat liver steroid sulfatase activity
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