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4'-Hydroxyacetophenone, 99%, Thermo Scientific Chemicals
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Catalog number A11974.36
also known as A11974-36
Price (USD)/ Each
151.65
Online exclusive
168.00 Save 16.35 (10%)
-
Quantity:
500 g
Price (USD)/ Each
151.65
Online exclusive
168.00 Save 16.35 (10%)
4'-Hydroxyacetophenone, 99%, Thermo Scientific Chemicals
Catalog numberA11974.36
Price (USD)/ Each
151.65
Online exclusive
168.00 Save 16.35 (10%)
-
Chemical Identifiers
CAS99-93-4
IUPAC Name1-(4-hydroxyphenyl)ethan-1-one
Molecular FormulaC8H8O2
InChI KeyTXFPEBPIARQUIG-UHFFFAOYSA-N
SMILESCC(=O)C1=CC=C(O)C=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Pale cream to cream to pale brown or pink
FormCrystals or powder or crystalline powder or flakes
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Melting Point (clear melt)105.0-112.0?C
4?-Hydroxyacetophenone has been used as ketone component in the preparation of 1-aryl-3-phenethylamino-1-propanone hydrochlorides, potential cytotoxic agents, via Mannich reactions.
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
4′-Hydroxyacetophenone has been used as ketone component in the preparation of 1-aryl-3-phenethylamino-1-propanone hydrochlorides, potential cytotoxic agents, via Mannich reactions.
Solubility
Soluble in 95% Ethanol. Slightly soluble in water.
Notes
Store at room temperature. Keep away from oxidizing agents.
4′-Hydroxyacetophenone has been used as ketone component in the preparation of 1-aryl-3-phenethylamino-1-propanone hydrochlorides, potential cytotoxic agents, via Mannich reactions.
Solubility
Soluble in 95% Ethanol. Slightly soluble in water.
Notes
Store at room temperature. Keep away from oxidizing agents.
RUO – Research Use Only
General References:
- Dick B. Janssen. Substrate Specificity and Enantioselectivity of 4-Hydroxyacetophenone Monooxygenase. Appl. Environ. Microbiol. 2003, 69 (1),419-426.
- W.B Gurnule.; P.K Rahangdale.; L.J Paliwal.; R.B Kharat. Synthesis, characterization and ion-exchange properties of 4-hydroxyacetophenone, biuret and formaldehyde terpolymer resins. React. Funct. Polym. 2003, 55 (3),255-265.