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| Classification | Chemical reagent >> Organic reagent >> Aromatic ketone |
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| Name | 4'-Chloropropiophenone |
| Synonyms | 1-(4-Chlorophenyl)-1-propanone |
| Molecular Structure | ![]() |
| Molecular Formula | C9H9ClO |
| Molecular Weight | 168.62 |
| CAS Registry Number | 6285-05-8 |
| EC Number | 228-511-6 |
| SMILES | CCC(=O)C1=CC=C(C=C1)Cl |
| Solubility | Insoluble (water) |
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| Density | 1.151 g/mL |
| Melting point | 34-37 ºC |
| Boiling point | 95-97 ºC (1 mmHg) |
| Flash point | 113 ºC |
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| Hazard Statements | H315-H319 Details | ||||||||||||||||||||||||||||||||
| Precautionary Statements | P264-P264+P265-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364 Details | ||||||||||||||||||||||||||||||||
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| SDS | Available | ||||||||||||||||||||||||||||||||
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4'-Chloropropiophenone is synthesized by organic chemistry methods aimed at modifying the structure of propiophenone, a simple aromatic ketone. The addition of a chlorine atom at the para position (4') of the benzene ring changes its chemical properties, enhancing its usefulness in tailor-made molecular applications. Chemically, the molecular formula of 4'-chloropropiophenone is C9H9ClO. It consists of a benzene ring attached to a keto group (C=O) and a chlorine atom (-Cl) located on the fourth carbon of the benzene ring. This structure gives it unique reactivity and solubility, which influences its use in organic synthesis and chemical transformations. The industrial applications of 4'-chloropropiophenone are diverse and cover several key areas. In medicinal chemistry, it serves as a precursor for the synthesis of various drug intermediates and active pharmaceutical ingredients (APIs). It serves as a building block in organic synthesis to create more complex molecules with specific pharmacological properties. In research laboratories, 4'-chloropropiophenone is used as a chemical reagent and intermediate to study new chemical reactions and develop new materials. Its structural versatility and ability to be selectively modified are valuable for understanding structure-activity relationships (SAR) and optimizing synthetic routes. In the specialty chemicals industry, 4'-chloropropiophenone is used to produce specialty polymers, agrochemicals, and flavoring agents. Its inclusion in specific formulations can improve product performance and stability, meeting the stringent quality standards and regulatory requirements of global markets. References 2008. Synthesis of rimonabant regioisomer. Monatshefte für Chemie - Chemical Monthly, 139(5). DOI: 10.1007/s00706-008-0903-7 2017. Nickel-Catalyzed Addition of Arylboronic Acids to Alkyl Nitriles for Synthesis of Aryl Ketones in Fluorinated Solvent. Synlett, 28(14). DOI: 10.1055/s-0036-1589137 2024. A comprehensive review on synthetic strategy and MOA of marketed drugs having therapeutically potential chemical entity pyrazole. Journal of the Iranian Chemical Society, 21(5). DOI: 10.1007/s13738-024-03095-7 |
| Market Analysis Reports |
| List of Reports Available for 4'-Chloropropiophenone |