4-(Trifluoromethoxy)benzaldehyde
Names
[ CAS No. ]:
659-28-9
[ Name ]:
4-(Trifluoromethoxy)benzaldehyde
[Synonym ]:
MFCD00041530
Benzaldehyde, 4-(trifluoromethoxy)-
EINECS 211-531-4
4-OCF3PhCHO
trifluoromethoxy-4 benzaldehyde
α,α,α-Trifluoro-p-anisaldehyde
4-trifluoromethoxybenzaldehyde
VHR DOXFFF
p-(Trifluoromethoxy)benzaldehyde
4-(Trifluoromethoxy)benzaldehyde
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
194.6±35.0 °C at 760 mmHg
[ Molecular Formula ]:
C8H5F3O2
[ Molecular Weight ]:
190.119
[ Flash Point ]:
70.6±0.0 °C
[ Exact Mass ]:
190.024170
[ PSA ]:
26.30000
[ LogP ]:
2.73
[ Vapour Pressure ]:
0.4±0.4 mmHg at 25°C
[ Index of Refraction ]:
1.479
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 ]:
Xn:Harmful;
[ Risk Phrases ]:
R22;R36/38
[ Safety Phrases ]:
S26-S36/37/39-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
29130000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2913000090
[ Summary ]:
HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0%
Articles
Acta Crystallogr. Sect. E Struct. Rep. Online 69(2) , o264-o264, (2013)
In the title compound, C(14)H(9)F(3)N(2)O, the best planes of the benzimidazole group and benzene ring form a dihedral angle of 26.68 (3)°. In the crystal, N-H⋯N hydrogen bonds link the mol-ecules int...
Broad-spectrum antiviral activity including human immunodeficiency and hepatitis C viruses mediated by a novel retinoid thiosemicarbazone derivative.Eur. J. Med. Chem. 46(5) , 1656-64, (2011)
Aromatic aldehyde-derived thiosemicarbazones 4-6, the S-substituted modified thiosemicarbazones 7/8, and a vitamin A-derived (retinoid) thiosemicarbazone derivative 12 were investigated as inhibitors ...
Synthesis of novel azo compounds containing 5(4H)-oxazolone ring as potent tyrosinase inhibitors.Bioorg. Med. Chem. 21(7) , 2088-92, (2013)
Six new azo dyes containing of 5(4H)-oxazolone ring were prepared by diazotization of 4-aminohippuric acid and coupling with N,N-dimethylaniline, 1-naphthol and 2-naphthol and condensation with 4-fluo...