4-(Trifluoromethoxy)benzaldehyde structure
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Common Name | 4-(Trifluoromethoxy)benzaldehyde | ||
|---|---|---|---|---|
| CAS Number | 659-28-9 | Molecular Weight | 190.119 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 194.6±35.0 °C at 760 mmHg | |
| Molecular Formula | C8H5F3O2 | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 70.6±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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2-[4-(Trifluoro-meth-oxy)phen-yl]-1H-benzimidazole.
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 into infinite chains parallel to the c axis. Stacking inter-ac... |
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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 of human hepatitis C virus (HCV) subgenomic RNA replicon Hu... |
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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-fluoro benzaldehyde or 4-trifluoromethoxy benzaldehyde. The new... |
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(E)-2-[4-(Trifluoro-meth-oxy)benzyl-idene]indan-1-one.
Acta Crystallogr. Sect. E Struct. Rep. Online 67(8) , o2147-o2147, (2011) In the title compound, C(17)H(11)F(3)O(2), the dihydro-indene ring is approximately planar with a maximum deviation of 0.024 (2) Å and makes a dihedral angle of 3.17 (8) Å with the adjacent benzene ring. In the crystal, mol-ecules are inter-connected by C-H⋯O... |
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A Versatile Synthesis of 4, 5-Dihydropyrrolo [1, 2-a] quinoxalines. Abonia R, et al.
J. Heterocycl. Chem. 38(3) , 671-4, (2001)
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