Name | 7-Hydroxy-4-(trifluoromethyl)coumarin |
Synonyms | TFMU TIMTEC-BB SBB006559 TRIFLUOROMETHYLUMBELLIFERONE 4-(TRIFLUOROMETHYL)UMBELLIFERON 4-(TRIFLUOROMETHYL)UMBELLIFERONE 7-HYDROXY-4-(TRIFLUOROMETHYL)COUMARIN 7-Hydroxy-4-(trifluoromethyl)coumarin 7-HYDROXY-4-TRIFLUOROMETHYL-CHROMEN-2-ONE 7-HYDROXY-4-(TRIFLUOROMETHYL)-2H-CHROMEN-2-ONE 7-Hydroxy-4-(trifluoromethyl)-2H-chromen-2-one 7-Hydroxy-4-(trifluoromethyl)-2H-1-benzopyran-2-one 2H-1-Benzopyran-2-one, 7-hydroxy-4-(trifluoromethyl)- |
CAS | 575-03-1 |
EINECS | 124-586-5 |
InChI | InChI=1/C10H5F3O3/c11-10(12,13)7-4-9(15)16-8-3-5(14)1-2-6(7)8/h1-4,14H |
InChIKey | CCKWMCUOHJAVOL-UHFFFAOYSA-N |
Molecular Formula | C10H5F3O3 |
Molar Mass | 230.14 |
Density | 1.4435 (estimate) |
Melting Point | 178-180 °C (lit.) |
Boling Point | 311.4±42.0 °C(Predicted) |
Flash Point | 142.2°C |
Solubility | DMF: soluble |
Vapor Presure | 0.000308mmHg at 25°C |
Maximum wavelength(λmax) | 330nm(Toluene)(lit.) |
BRN | 210932 |
pKa | 7.23±0.20(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.546 |
MDL | MFCD00037578 |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R25 - Toxic if swallowed |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
FLUKA BRAND F CODES | 8-10 |
HS Code | 29322090 |
Hazard Class | IRRITANT |
introduction | research shows that 7-hydroxy -4-trifluoromethyl coumarin compounds have a great improvement over 4-methyl -7 hydroxy coumarin derivatives in terms of water solubility and antibacterial activity, it has good antibacterial activity against rice sheath blight fungus, cucumber anthracnose fungus, strawberry gray mold fungus, wheat scab fungus, apple spot fungus, tomato early blight fungus, and has broad-spectrum antibacterial activity. It is expected to develop into a class of antibacterial agents with broad application prospects. |
preparation method | 3-hydroxyphenol (11g,100mmol) and ethyl trifluoroacetoacetate (15mL,100mmol) were added to concentrated phosphoric acid (52mL,85%). After stirring at room temperature for 12 hours, the reaction mixture was poured into 150mL of water. The crude product was collected by filtration and purified by recrystallization in ethanol. |
use | suitable for use as pH indicator |