Name | 4-Chloro-4'-hydroxybenzophenone |
Synonyms | LABOTEST-BB LT00248477 4-p-Chlorobenzoylphenol 4-(4-CHLOROBENZOYL)PHENOL 4-Chloro-4-Hydroxybenzophenone 4-Chloro-4'-hydroxybenzophenon 4-Chloro-4'-hydroxybenzophenone 4-hydroxy-4'-chloro-benophenone 4-chloro-4'-hydroxy benzophenone 4-(4-Chlorobenzoyl)-4-Hydroxypiperidine (4-chlorophenyl)(4-hydroxyphenyl)methanone (4-Chlorophenyl)(4-hydroxyphenyl)-Methanone 4-Chloro-4'-Hydroxybenzophenone 4-Hydroxy-4'-Chlorobenzophenone |
CAS | 42019-78-3 |
EINECS | 255-627-4 |
InChI | InChI=1/C13H9ClO2/c14-11-5-1-9(2-6-11)13(16)10-3-7-12(15)8-4-10/h1-8,15H |
Molecular Formula | C13H9ClO2 |
Molar Mass | 232.66 |
Density | 1.2082 (rough estimate) |
Melting Point | 177-181 °C |
Boling Point | 257 °C (13 mmHg) |
Flash Point | 100 °C |
Solubility | DMSO (Slightly), Methanol (Slightly, Sonicated) |
Vapor Presure | 4.17E-07mmHg at 25°C |
Appearance | White crystal |
Color | Pale Beige to Light Brown |
BRN | 2049956 |
pKa | 7.68±0.15(Predicted) |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | 1.5434 (estimate) |
MDL | MFCD00002357 |
Physical and Chemical Properties | Melting point 177-181°C boiling point 257°C (13 torr) flash point 100°C |
Use | As a pharmaceutical fenofibrate Intermediate |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S37/39 - Wear suitable gloves and eye/face protection S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
HS Code | 29144000 |
Hazard Note | Irritant |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
use | The impurity of Fenofibric acid (42017-89-0), the active metabolite of fenofibrate which increases Apolipoprotein A- I holmium ediated High-Density Lipoprotein Biogenesis by enhancing transcription of ATP-Bin ding cassette transporter A1 gene in a liver X receptor holmium back ependent manner. used as pharmaceutical fenofibrate intermediate |
Production method | 1. The reaction method of p-chlorobenzoyl chloride and anisole? ??? After the reaction of p-chlorobenzoyl chloride and anisole, it is prepared by hydrolysis and demethylation. 2. reaction method between p-chlorobenzoyl chloride and phenol????? Dissolve 9.4g(0.1mol) of phenol in 4ml of 10% sodium hydroxide solution, add 14ml(0.110mol) of p-chlorobenzoyl chloride dropwise at 40~45 ℃, add it within 30min, and react at the same temperature for 1h. Cool to room temperature, filter and dry to obtain 22.3g of phenyl p-chlorobenzoate. The yield is 96%, and the melting point is 99~101 ℃. |