ChemicalBook Product Catalog Chemical Reagents Organic reagents Thiourea 1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA

1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA

1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA Basic information
Product Name:1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA
Synonyms:1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA;1-(4-(trifluoroMethoxy)phenyl)thiourea;N-[4-(trifluoromethoxy)phenyl]thiourea;1-[4-(Trifluoromethoxy)phenyl]-2-thiourea 97%;1-[4-(Trifluoromethoxy)phenyl]-2-thiourea97%;1-(Carbamothioylamino)-4-(trifluoromethoxy)benzene, 1-Thioureido-4-(trifluoromethoxy)benzene;4-(Trifluoromethoxy)phenylthiourea 97%;Riluzole Impurity 15
CAS:142229-74-1
MF:C8H7F3N2OS
MW:236.21
EINECS:
Product Categories:Sulphur Derivatives
Mol File:142229-74-1.mol
1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA Structure
1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA Chemical Properties
Melting point 138-140°C
Boiling point 269.5±50.0 °C(Predicted)
density 1.495±0.06 g/cm3(Predicted)
storage temp. -20°C Freezer
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka12.53±0.70(Predicted)
color White
CAS DataBase Reference142229-74-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
Hazard Note Irritant
HS Code 2930909899
MSDS Information
1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA Usage And Synthesis
Uses1-?(4-?(Trifluoromethoxy)?phenyl)?-?2-?thiourea Is used as a reagent in the synthesis of 2-aminothiazole derivatives which act as sphingosine kinase inhibitors. These 2-aminothiazole derivatives thus act as anticancer and anti-inflammatory agents.
1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA Preparation Products And Raw materials
1-(4-METHYLPIPERAZINYL)-3-(4-(TRIFLUOROMETHOXY)PHENYL)THIOUREA 1-(2-(2,4-DICHLOROPHENOXY)PROPIONYL)-4-(4-(TRIFLUOROMETHOXY)PHENYL)THIOSEMICARBAZIDE 1-(2-(3-CHLORO-5-(TRIFLUOROMETHYL)(2-PYRIDYLTHIO))ACETYL)-4-(4-(TRIFLUOROMETHOXY)PHENYL)THIOSEMICARBAZIDE 1-(2-INDOL-3-YLETHYL)-3-(4-(TRIFLUOROMETHOXY)PHENYL)THIOUREA 3-(2,3,6-TRIAZINO[5,4-B]INDOL-3-YLTHIOMETHYL)-4-(4-(TRIFLUOROMETHOXY)PHENYL)-1,2,4-TRIAZOLINE-5-THIONE (4-(DIPHENYLMETHYL)PIPERAZINYL)((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHANE-1-THIONE 4-(4-TRIFLUOROMETHOXYPHENYL)THIOSEMICARBAZIDE (6-METHYL(1,2,3,4-TETRAHYDROQUINOLYL))((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHANE-1-THIONE 3-(4-TRIFLUOROMETHOXYPHENYL)-2-THIOXO-1,3-DIHYDROQUINAZOLIN-4-ONE METHYL 4-((N-((THIOXO((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHYL)AMINO)CARBAMOYL)METHOXY)BENZOATE N1-[4-(TRIFLUOROMETHOXY)PHENYL]-2-(2-BROMO-1-PHENYLETHYLIDENE)-1-(2-HYDROXYETHYL)HYDRAZINE-1-CARBOTHIOAMIDE ((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)(4-(5-(TRIFLUOROMETHYL)(2-PYRIDYL))PIPERAZINYL)METHANE-1-THIONE BUTTPARK 12\07-45 2-METHYL-4-(4-(TRIFLUOROMETHOXY)PHENYL)THIOSEMICARBAZIDE 3-PHENYL-N-(THIOXO((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHYL)PROP-2-ENAMIDE 1-(4-(TRIFLUOROMETHOXY)PHENYL)-2-THIOUREA ETHYL 2-((THIOXO((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHYL)AMINO)-4,5,6,7-TETRAHYDROBENZO[B]THIOPHENE-3-CARBOXYLATE (4-(THIOXO((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHYL)PIPERAZINYL)((4-(TRIFLUOROMETHOXY)PHENYL)AMINO)METHANE-1-THIONE
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