1-(4-CHLOROPHENYL)-3-PHENYL-2-PROPEN-1-ONE
4'-Chlorochalcone
CAS: 956-02-5
Molecular Formula: C15H11ClO
1-(4-CHLOROPHENYL)-3-PHENYL-2-PROPEN-1-ONE - Names and Identifiers
| Name | 4'-Chlorochalcone |
| Synonyms | 4'-Chlorochalcone BENZILIDENE-4-CHLOROACETOPHENONE 1-(4-CHLOROPHENYL)-3-PHENYL-2-PROPEN-1-ONE (E)-1-(4-CHLOROPHENYL)-3-PHENYLPROP-2-EN-1-ONE |
| CAS | 956-02-5 |
1-(4-CHLOROPHENYL)-3-PHENYL-2-PROPEN-1-ONE - Physico-chemical Properties
| Molecular Formula | C15H11ClO |
| Molar Mass | 242.71 |
| Density | 1.202±0.06 g/cm3(Predicted) |
| Melting Point | 97-101 °C(lit.) |
| Boling Point | 386.8±42.0 °C(Predicted) |
| Storage Condition | Room Temprature |
| MDL | MFCD00016343 |
1-(4-CHLOROPHENYL)-3-PHENYL-2-PROPEN-1-ONE - Risk and Safety
| 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 - Wear suitable gloves. |
1-(4-CHLOROPHENYL)-3-PHENYL-2-PROPEN-1-ONE - Introduction
4 '-Chlorochalcone is an organic compound whose chemical formula is C15H9ClO. The following is a description of some of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: 4 '-Chlorochalcone are colorless crystals or white crystalline powder.
-Melting point: about 113-115°C.
-Solubility: 4 '-Chlorochalcone can be dissolved in organic solvents such as ethanol and dimethylformamide, but the solubility in water is low.
Use:
- 4 '-Chlorochalcone is commonly used as an intermediate in organic synthesis. It can be used to synthesize compounds with bactericidal, antioxidant, anti-tumor, anti-inflammatory and antiviral activities.
- 4 '-Chlorochalcone has electron attractive chlorine atom, which makes it have good reactivity and can be used for the synthesis of oxygen nitrogen heterocycles.
Preparation Method:
- 4 '-Chlorochalcone can be synthesized by an Aldor reaction in an acidic or alkaline medium. Specific methods include the reaction of aldehydes with benzoic anhydride to form 4 '-Chlorochalcone.
Safety Information:
- 4 '-Chlorochalcone is an organic synthetic intermediate with certain toxicity. An appropriate amount of protective measures should be taken during the operation, such as wearing protective glasses, gloves and laboratory coats.
-The compound may be irritating to the human body, so contact with skin and eyes should be avoided. In case of contact, flush with plenty of water and seek medical attention as soon as possible.
-During operation and storage, avoid contact with harmful substances such as oxidants, strong acids and strong bases to prevent dangerous reactions.
Nature:
-Appearance: 4 '-Chlorochalcone are colorless crystals or white crystalline powder.
-Melting point: about 113-115°C.
-Solubility: 4 '-Chlorochalcone can be dissolved in organic solvents such as ethanol and dimethylformamide, but the solubility in water is low.
Use:
- 4 '-Chlorochalcone is commonly used as an intermediate in organic synthesis. It can be used to synthesize compounds with bactericidal, antioxidant, anti-tumor, anti-inflammatory and antiviral activities.
- 4 '-Chlorochalcone has electron attractive chlorine atom, which makes it have good reactivity and can be used for the synthesis of oxygen nitrogen heterocycles.
Preparation Method:
- 4 '-Chlorochalcone can be synthesized by an Aldor reaction in an acidic or alkaline medium. Specific methods include the reaction of aldehydes with benzoic anhydride to form 4 '-Chlorochalcone.
Safety Information:
- 4 '-Chlorochalcone is an organic synthetic intermediate with certain toxicity. An appropriate amount of protective measures should be taken during the operation, such as wearing protective glasses, gloves and laboratory coats.
-The compound may be irritating to the human body, so contact with skin and eyes should be avoided. In case of contact, flush with plenty of water and seek medical attention as soon as possible.
-During operation and storage, avoid contact with harmful substances such as oxidants, strong acids and strong bases to prevent dangerous reactions.
Last Update：2024-04-10 22:29:15
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