CAS 1023-17-2: 4'-METHOXY-2-PHENYLACETOPHENONE
Formula:C15H14O2
InChI:InChI=1/C15H14O2/c1-17-14-9-7-13(8-10-14)15(16)11-12-5-3-2-4-6-12/h2-10H,11H2,1H3
SMILES:COc1ccc(cc1)C(=O)Cc1ccccc1
Synonyms:- 4-Methoxyphenylbenzyl Ketone
- Deoxy-4-Methoxybenzoin
- Benzyl 4-Methoxyphenyl Ketone
- Nsc26658
- 1-(4-Methoxyphenyl)-2-Phenylethanone
- 1-(4-Methoxyphenyl)acetophenone
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Found 6 products.
1-(4-Methoxyphenyl)acetophenone
CAS:Controlled ProductApplications An intermediate for the synthesis of many biologically active molecules including receptor ligands and enzyme inhibitors References Chesworth, R., et al.: Bioorg. Med. Chem. Lett., 15, 5562 (2005), Gupta, A., et al.: Med. Chem., 3, 241 (2007), Ramajayam, R., et al.: Eur. J. Med. Chem., 43, 2004 (2008),Formula:C15H14O2Color and Shape:NeatMolecular weight:226.274'-Methoxy-2-phenylacetophenone
CAS:4'-Methoxy-2-phenylacetophenonePurity:98+%Molecular weight:226.27g/molEthanone, 1-(4-methoxyphenyl)-2-phenyl-
CAS:Formula:C15H14O2Purity:98%Color and Shape:SolidMolecular weight:226.27051-(4-Methoxyphenyl)-2-phenylethanone
CAS:Formula:C15H14O2Purity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:226.281-(4-Methoxyphenyl)acetophenone
CAS:1-(4-Methoxyphenyl)acetophenone is an enantiomer of the naturally occurring compound melatonin. It has been shown to have insecticidal activities and is effective against insects at temperatures below 10°C. 1-(4-Methoxyphenyl)acetophenone undergoes a cyclodehydration reaction with loss of water and formation of a six-membered ring, which is catalysed by acid, inorganic bases, or metal salts. This reaction can be modified by substituting diacids, halides, or electrolysing agents for water. The resulting products are unsymmetrical and soluble in organic solvents.Formula:C15H14O2Purity:Min. 95%Color and Shape:PowderMolecular weight:226.27 g/mol4'-Methoxy-2-phenylacetophenone
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:226.27499389648438
