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4-(4-Hydroxyphenyl)-2-butanone | CAS:5471-51-2
4-(4-Hydroxyphenyl)-2-butanone
  • Name:4-(4-Hydroxyphenyl)-2-butanone
  • CAS:5471-51-2
  • Synonyms:1-(4-Hydroxyphenyl)-3-butanone; 4-(4-Hydroxyphenyl)butan-2-one; Raspberry keton; Frambinone
  • Molecular Formula:C10H12O2
  • Molecular Weight:164.20
  • EINESC:226-806-4

Description

Properties

Melting point 82-84 ºC
Boiling point 200 ºC

Safety

Symbol(GHS) Xn
Hazard Codes R22

SDS

Source SDS/MSDS Samples
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Articles
Peer-Reviewed Papers
Tyrosine Hydroxylase Inhibitors. Synthesis and Activity of Substituted Aromatic Amino Acids. Saari WS, et al. Journal of Medicinal Chemistry, 10(6), 1008-1014 (1967) Polystyrene-Supported p-Toluenesulfonic Acid: A New, Highly Efficient, and Recyclable Catalyst for the Synthesis of Hydropyridine Derivatives under Solvent-Free Conditions.Reddy MV and Jeong YT. Synlett, 23(20), 2985-2991 (2012) Fluorinated derivatives of titanocene Y: synthesis and cytotoxicity studies. Claffey J, et al. European Journal of Organic Chemistry, 26, 4074-4082 (2008) Chiral building blocks: enantioselective syntheses of benzyloxymethyl phenyl propionic acids.Jack G Parsons et al.Molecules (Basel, Switzerland), 9(6), 449-458 (2007-11-17) Synthesis of 1, 3-Bis (hydroxy-halogenophenyl)-propane-1, 3-diamines and their Pt (II) Complexes, Syntheses of the Ligands. Kammermeier T and Wiegrebe W. Arch. Pharm. (Weinheim), 327, 547-561 (1994) Indium trifluoride: A highly efficient catalyst for the synthesis of fluorine-containing 2, 4, 5-trisubstituted imidazoles under solvent-free conditions. Reddy MV and Jeong YT. Journal of Fluorine Chemistry, 142, 45-51 (2012) Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives. Hatti I, et al. Medicinal Chemistry Research, 24(8), 3305-3313 (2015)
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