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Thermo Scientific Chemicals
3'-Hydroxyacetophenone, 98%
CAS: 121-71-1 | C8H8O2 | 136.15 g/mol
化学物質識別子
CAS121-71-1
IUPAC Name1-(3-hydroxyphenyl)ethan-1-one
Molecular FormulaC8H8O2
InChI KeyLUJMEECXHPYQOF-UHFFFAOYSA-N
SMILESCC(=O)C1=CC=CC(O)=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Cream to pale yellow
FormPowder
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)92.0-98.0?C
3’Hydroxyacetophenone is used in the preparation of chalcones and flavonoids, which finds application as an anti-tuberculosis agent and antileishmanial chaocones. It is also involved in the preparation of phenylephrine. Further, it is an active component of castoreum, which is used as a tincture in some perfumes and as a food additive.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3’Hydroxyacetophenone is used in the preparation of chalcones and flavonoids, which finds application as an anti-tuberculosis agent and antileishmanial chaocones. It is also involved in the preparation of phenylephrine. Further, it is an active component of castoreum, which is used as a tincture in some perfumes and as a food additive.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Incompatible with strong oxidizing agents and bases.
3’Hydroxyacetophenone is used in the preparation of chalcones and flavonoids, which finds application as an anti-tuberculosis agent and antileishmanial chaocones. It is also involved in the preparation of phenylephrine. Further, it is an active component of castoreum, which is used as a tincture in some perfumes and as a food additive.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Incompatible with strong oxidizing agents and bases.
RUO – Research Use Only
General References:
- Tibbetts, K. M.; Bohinski, T.; Munkerup, K.; Tarazkar, M.; Levis, R. Controlling Dissociation of Alkyl Phenyl Ketone Radical Cations in the Strong-Field Regime through Hydroxyl Substitution Position. J. Phys. Chem. A 2014, 118 (37), 8170-8176.
- Rotas, G.; Niemi, M.; Tkachenko, N. V.; Zhao, S.; Shinohara, H.; Tagmatarchis, N. Organic-Inorganic Azafullerene-Gold C59N-Au Nanohybrid: Synthesis, Characterization, and Properties. Chem. Eur. J. 2014, 20 (45), 14729-14735.