Name | 4-Chlorophenyl cyclopropyl ketone |
Synonyms | 4-CHLOROBENZOYLCYCLOPROPANE (4-Chlorobenzoyl)cyclopropane 4-Chlorophenyl cyclopropyl ketone 4-CHLOROPHENYL CYCLOPROPYL KETONE P-CHLOROPHENYL CYCLOPROPYL KETONE CYCLOPROPYL-4-CHLOROPHENYL KETONE (4-Chlorophenyl)cyclopropylmethanone (4-CHLOROPHENYL)CYCLOPROPYLMETHANONE Methanone, (4-chlorophenyl)cyclopropyl- bis(4-chloro-2-cyclopropylphenyl)methanone |
CAS | 6640-25-1 |
EINECS | 229-655-2 |
InChI | InChI=1/C10H9ClO/c11-9-5-3-8(4-6-9)10(12)7-1-2-7/h3-7H,1-2H2 |
Molecular Formula | C10H9ClO |
Molar Mass | 180.63 |
Density | 1.16 |
Melting Point | 29-31°C(lit.) |
Boling Point | 135-137°C 10mm |
Flash Point | >230°F |
Vapor Presure | 0.00256mmHg at 25°C |
Appearance | powder to lump to clear liquid |
Color | White or Colorless to Yellow to Orange |
BRN | 2044845 |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | n20/D 1.5718(lit.) |
MDL | MFCD00001295 |
Physical and Chemical Properties | This product is solid or liquid, m. P. 29~31 ℃, B. P. 110~112 ℃ (1.34 kpa),n20D 1.5718, insoluble in water. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
WGK Germany | 3 |
melting point 29~31 ℃, boiling point 110~112 ℃(1. 33kPa), refractive index 1.5688(25 ℃).
obtained by the reaction of chloro-butyryl chloride with chlorobenzene, the yield is up to 68.5%.
This product is used for the synthesis of high biological activity of new type of pyrethroid pesticide cyclopropyl 4 chlorophenone oxime o(3 phenoxybenzyl) ether.
Net weight 50kg, plastic drum packaging.
NIST chemical information | information provided by: webbook.nist.gov (external link) |
Use | 4-chlorophenylcyclopropyl ketone is an intermediate of the insecticide fluorocyclourea. This product is used for the synthesis of new pyrethroid pesticide cyclopropyl-4-chlorophenone oxime-o-(3-phenoxybenzyl) ether with high biological activity. |
production method | is derived from the reaction of γ-chlorobutyryl chloride with chlorobenzene. The yield was 68.5%. The preparation method is obtained by the reaction of γ-chlorobutyryl chloride with chlorobenzene. Aluminum trichloride and chlorobenzene were added to the reactor, and a mixture of γ-chlorobutyryl chloride and Chlorobenzene was added dropwise with stirring, maintaining the temperature at 25 to 30 °c. After the addition was maintained for 30min, the reaction was poured into water to separate the oil layer, washed with water, dried over anhydrous magnesium sulfate, and the low boiling material was removed to give a brown oil. KOH was dissolved in methanol, and then added to the above distillation residue, stirred, cooled and filtered, the filter cake was washed with methanol, the filtrate was removed under reduced pressure, the residue was diluted with dichloromethane, washed with water, the oil layer was dried over anhydrous magnesium sulfate, the solvent was removed, and the product was distilled under reduced pressure. |