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Thermo Scientific Chemicals
2'-Hydroxy-5'-methylacetophenone, 98%
CAS: 1450-72-2 | C9H10O2 | 150.177 g/mol
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Catalog number A13136.06
also known as A13136-06
Price (USD)
52.65
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Online exclusive
Ends: 30-Jun-2026
62.10Save 9.45 (15%)
Each
Quantity:
5 g
Price (USD)
52.65
Special offer
Online exclusive
Ends: 30-Jun-2026
62.10Save 9.45 (15%)
Each
Chemical Identifiers
CAS1450-72-2
IUPAC Name1-(2-hydroxy-5-methylphenyl)ethan-1-one
Molecular FormulaC9H10O2
InChI KeyYNPDFBFVMJNGKZ-UHFFFAOYSA-N
SMILESCC(=O)C1=CC(C)=CC=C1O
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Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Assay (GC)≥97.5%
Melting Point (clear melt)44.0-50.0?C
Appearance (Color)Pale yellow
2'-Hydroxy-5'-methylacetophenone is used to produce 2-ethyl-4-methyl-phenol. It is used as an intermediate in organic synthesis.
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
2′-Hydroxy-5′-methylacetophenone is used to produce 2-ethyl-4-methyl-phenol. It is used as an intermediate in organic synthesis.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
2′-Hydroxy-5′-methylacetophenone is used to produce 2-ethyl-4-methyl-phenol. It is used as an intermediate in organic synthesis.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
Gheorghe Roman; Diana Nanu; Eugenia Comanita; Bogdan Comanita. Synthesis and reactivity of some mannich bases. VI. New arylamine mannich bases derived from 2-Hydroxy-5-methylacetophenone. Turk J. Chem. 2000, 24, 67-71