For research use only. Not for therapeutic Use.
Phenoxyacetone (Cat No.:I014569) is an organic compound. It consists of a phenyl group attached to an acetone moiety. Phenoxyacetone is commonly used as an intermediate in the synthesis of fragrances, perfumes, and cosmetics. It also finds application in the production of pharmaceuticals and other organic compounds. With its versatile chemical structure, phenoxyacetone serves as a valuable building block in various chemical reactions, contributing to the development of diverse products across industries such as fragrance, cosmetics, and pharmaceuticals.
| Catalog Number | I014569 |
| CAS Number | 621-87-4 |
| Synonyms | Phenoxyacetone; NSC 1876; NSC-1876; NSC1876;2-PropaNA, 1-phenoxy- |
| Molecular Formula | C9H10O2 |
| Purity | ≥95% |
| Target | Acetylcholinesterase inhibitor |
| Solubility | Soluble in DMSO |
| Storage | 2-8°C |
| IUPAC Name | 1-phenoxypropan-2-one |
| InChI | InChI=1S/C9H10O2/c1-8(10)7-11-9-5-3-2-4-6-9/h2-6H,7H2,1H3 |
| InChIKey | QWAVNXZAQASOML-UHFFFAOYSA-N |
| SMILES | CC(=O)COC1=CC=CC=C1 |
| Reference | </br> 1: Dafforn A, Neenan JP, Ash CE, Betts L, Finke JM, Garman JA, Rao M, Walsh K, Williams RR. Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propaNAs. Biochem Biophys Res Commun. 1982 Jan 29;104(2):597-602. PubMed PMID: 7073703.</br>2: Landquist JK. Oxidative cyclisation of ketone thiosemicarbazones. II. Derivatives of phenoxyacetone. J Chem Soc Perkin 1. 1970;2:323-4. PubMed PMID: 5460862. </br> </br> |
