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About This Item
Linear Formula:
BrCH2CH2CF3
CAS Number:
Molecular Weight:
176.96
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Ozone 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Phosphorus substituted hydroxylamine and hydroxamic acid derivatives: synthesis and reactivity.
Alonso C, et al.
ARKIVOC (Gainesville, FL, United States), 221-253 (2011)
Y Tanaka et al.
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
L W Lawrence Woo et al.
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
Tetrahedron Letters, 37, 5557-5557 (1996)
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