452807
Trichloro(3,3,3-trifluoropropyl)silane
97%
Synonym(s):
3,3,3-Trifluoropropyl-trichlorosilane
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About This Item
Linear Formula:
CF3CH2CH2SiCl3
CAS Number:
Molecular Weight:
231.50
UNSPSC Code:
12352001
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-744-2
Beilstein/REAXYS Number:
1748876
MDL number:
Assay:
97%
InChI key
WEUBQNJHVBMUMD-UHFFFAOYSA-N
InChI
1S/C3H4Cl3F3Si/c4-10(5,6)2-1-3(7,8)9/h1-2H2
SMILES string
FC(F)(F)CC[Si](Cl)(Cl)Cl
assay
97%
refractive index
n20/D 1.386 (lit.)
bp
114 °C (lit.)
density
1.419 g/mL at 25 °C (lit.)
functional group
fluoro
Quality Level
Related Categories
Application
Trichloro(3,3,3-trifluoropropyl)silane can be used as a precursor for the preparation of:
It can also be used as a silanizing agent to coat the inner surface of pipettes in order to investigate the electrical charging of droplets discharged from the micropipette.
- Fluorinated polyhedral oligomeric silsesquioxane (F-POSS) by base-catalyzed condensation.
- 3,3,3-Trifluoropropyltrimethoxysilane by alcoholysis reaction with methanol.
It can also be used as a silanizing agent to coat the inner surface of pipettes in order to investigate the electrical charging of droplets discharged from the micropipette.
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 3 - Skin Corr. 1B
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
113.7 °F - closed cup - (own results)
flash_point_c
45.4 °C - closed cup - (own results)
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Shifted transfer characteristics of organic thin film and single crystal FETs.
Synt. Metals, 146(3), 325-328 (2004)
Journal of the Electrochemical Society, 142, L11-L11 (1995)
Spontaneous electrical charging of droplets by conventional pipetting.
Scientific Reports, 3 (2013)
Alcoholysis synthesis of 3, 3, 3-trifluoropropyltrimethoxysilane by solvent method [J]
Biqian Jin
New Chemical Materials, 11 (2007)
Kyung Won Ro et al.
Electrophoresis, 24(18), 3253-3259 (2003-10-01)
Capillary electrochromatography (CEC) and preconcentration of neutral compounds have been realized on poly(dimethylsiloxane) (PDMS) microchips. The channels are coated with polyelectrolyte multilayers to avoid absorption of hydrophobic analytes into PDMS. The structures of a microchip include an injector and a
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