T63703
α,α,α-Trifluorotoluene
≥99%
Synonym(s):
Benzotrifluoride
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About This Item
Linear Formula:
C6H5CF3
CAS Number:
Molecular Weight:
146.11
Beilstein:
1906908
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.21
Assay:
≥99%
bp:
102 °C (lit.)
vapor pressure:
38.83 mmHg
Recommended Products
vapor density
5.04 (vs air)
Quality Level
vapor pressure
38.83 mmHg
Assay
≥99%
form
liquid
expl. lim.
0.34-6.3 %
refractive index
n20/D 1.414 (lit.)
bp
102 °C (lit.)
mp
−29 °C (lit.)
density
1.19 g/mL at 20 °C (lit.)
SMILES string
FC(F)(F)c1ccccc1
InChI
1S/C7H5F3/c8-7(9,10)6-4-2-1-3-5-6/h1-5H
InChI key
GETTZEONDQJALK-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2 - Flam. Liq. 2 - STOT RE 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
46.4 °F - closed cup
Flash Point(C)
8 °C - closed cup
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Neuropharmacology, 48(4), 479-491 (2005-03-10)
Glutamate transporters rapidly take up synaptically released glutamate and maintain the glutamate concentration in the synaptic cleft at a low level. (2S, 3S)-3-[3-[4-(trifluoromethyl)benzoylamino]benzyloxy]aspartate (TFB-TBOA) is a novel glutamate transporter blocker that potently suppresses the activity of glial transporters. TFB-TBOA inhibited
[Hygienic standardization of benzotrifluoride level in reservoir water].
V I Antonova et al.
Gigiena i sanitariia, (2)(2), 86-87 (1985-02-01)
Bhawani Singh Rathore et al.
Bioorganic & medicinal chemistry, 14(16), 5678-5682 (2006-05-03)
7-Chloro-5-trifluoromethyl/7-fluoro/7-trifluoromethyl-4H-1,4-benzothiazines have been synthesized by 2-amino-5-fluoro/5-trifluoromethyl/5-chloro-3-trifluoromethyl benzenethiols condensed with beta-diketone/beta-ketoesters in the presence of DMSO involving oxidative cyclization. Pharmacological activities have also been included.
Hidetoshi Yamada et al.
Carbohydrate research, 337(7), 581-585 (2002-03-23)
A glycosylation reaction induced by copper(II) trifluoromethanesulfonate is described. Using benzotrifluoride as the reaction solvent, five kinds of glycosyl donors, a glucosyl chloride, a fluoride, a trichloroacetimidate, a 1-O-acetyl compound, and a lactol were activated to give the corresponding glucosides.
C Yost et al.
Applied occupational and environmental hygiene, 15(1), 165-170 (2000-03-11)
Three solvents (OXSOL 10, monochlorotoluene or mixed isomers of 1- chloro-2-methyl benzene and 1-chloro-4-methyl benzene; OXSOL 100, parachlorobenzotrifluoride or 1-chloro-4-(trifluoromethyl) benzene; and OXSOL 2000, benzotrifluoride or trifluoromethyl benzene) produced by Occidental Chemical Corporation (Niagara Falls, NY) were considered as candidates
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