Name | 7-chloroquinolin-4-ol |
Synonyms | 7-chloroquinolin-4-ol 7-Chloroquinolin-4-ol 7-CHLORO-4-QUINOLINOL 7-chloro-4-quinolinol 4-Quinolinol, 7-chloro- 7-CHLORO-4-HYDROQUINOLINE 7-CHLORO-4(1H)-QUINOLINONE 7-chloroquinolin-4(1H)-one 4-Hydroxy-7-chloroquinoline 7-Chloro-4-hydroxyquinoline 7-CHLORO-4-HYDROXYQUINOLINE 7-Chloro-4(1H)-quinolinone([2383-97-8]) |
CAS | 86-99-7 |
EINECS | 201-715-2 |
InChI | InChI=1/C9H6ClNO/c10-6-1-2-7-8(5-6)11-4-3-9(7)12/h1-5H,(H,11,12) |
Molecular Formula | C9H6ClNO |
Molar Mass | 179.6 |
Density | 1.412±0.06 g/cm3(Predicted) |
Melting Point | 276-279°C(lit.) |
Boling Point | 348.5±22.0 °C(Predicted) |
Flash Point | 136.9°C |
Vapor Presure | 0.000966mmHg at 25°C |
BRN | 125356 |
pKa | 3.86±0.40(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.608 |
MDL | MFCD00006778 |
Physical and Chemical Properties | Colorless needle-like crystals. Melting point 276-280 ℃, micro-soluble in cold water, soluble in hot water. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
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 |
uses | pharmaceutical and dye intermediates. It can be used to synthesize the anti-cancer drug chloroquine phosphate. |
production method | in the laboratory, can be heated 7-chloro-4-hydroxyquinoline-3-carboxylic acid derived. A large number of bubbles were generated when heated to 250-270 °c. When the evolution of the bubbles stopped, it was cooled, and the reaction solution was decanted. After cooling, a crude solid product was obtained, which was recrystallized with water. The crude yield was 98%. Industrial production can be started from M-chloroaniline, by condensation, cyclization, hydrolysis and 7-chloro-4-hydroxyquinoline-3-carboxylic acid, which is heated together with paraffin oil to eliminate, the upper layer of paraffin oil in the product was removed to obtain 7-chloro-4-hydroxyquinoline. |