Name | 3-hydroxyisoquinoline |
Synonyms | 3-Isoquinolinol 3-ISOQUINOLINOL Isoquinolin-3-ol isoquinolin-3-ol 3(2H)-Isoquinolinone isoquinolin-3(2H)-one Isoquinolin-3(2H)-one 3-HYDROXYISOQUINOLINE 3-Hydorxyisoquinoline 3-hydroxyisoquinoline 2,3-dihydroisoquinolin-3-one Isoquinolin-3-ol, 3-Hydroxy-2-azanaphthalene |
CAS | 7651-81-2 |
InChI | InChI=1/C9H7NO/c11-9-5-7-3-1-2-4-8(7)6-10-9/h1-6H,(H,10,11) |
Molecular Formula | C9H7NO |
Molar Mass | 145.16 |
Density | 1.23±0.1 g/cm3(Predicted) |
Melting Point | 192-194 °C (lit.) |
Boling Point | 551.9±23.0 °C(Predicted) |
Flash Point | 319.4°C |
Vapor Presure | 3.16E-12mmHg at 25°C |
BRN | 113230 |
pKa | 11.06±0.20(Predicted) |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | 1.642 |
MDL | MFCD00075524 |
Risk Codes | R22 - Harmful if swallowed R41 - Risk of serious damage to eyes |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
HS Code | 29334900 |
Hazard Note | Irritant |
preparation | The resealable reaction tube containing the magnetic follower was sealed with a rubber spacer. The tube was dried with a flame under a flow of argon. tBu3P. HBF4(10.9 mg, 0.0377 mmol) and Pd2(dba)3(17.3 mg, 0.0189 mmol) were added to the tube. The aryl bromide (83.6 mg) was dissolved in anhydrous toluene (0.9 ml) . The resulting solution was added to the tube via syringe. Tert-butyl acetate (87.6 mg) was added to the tube. The reaction mixture was cooled to -78°C. The reaction mixture was degassed with argon for 15 min. Degassed LiHDMS solution (0.942 ml, 1m in toluene) was added to the mixture via syringe. The reaction mixture was degassed for 15 min. Replace the rubber diaphragm with a screw cap. The reaction was stirred at room temperature for 16 hours. The reaction was quenched by the addition of saturated aqueous NaHCO3 (25 mL). The aqueous layer was extracted with Et2O (3 x 25 mL). The combined organics were dried over Na2SO4. The combined organics were filtered. The solvent was removed in vacuo. The product was purified by flash column chromatography [petroleum/EtOAc 50:1, fractionated to 5:1]. |
Use | 3-hydroxyisoquinoline is a compound used in a polymer mixture of polyvinyl alcohol (PVA) and Nile red, white light can be generated by Forster resonance energy transfer. Can be used as organic, pharmaceutical intermediates. |