2'-HYDROXY-6'-METHOXYACETOPHENONE
2'-HYDROXY-6'-METHOXYACETOPHENONE Basic information
- Product Name:
- 2'-HYDROXY-6'-METHOXYACETOPHENONE
- Synonyms:
-
- 6'-Hydroxy-2'-methoxyacetophenone
- Acetophenone, 2'-hydroxy-6'-methoxy-
- 2'-Hydroxy-6'-methoxyacetophenone 98%
- 2'-HYDROXY-6'-METHOXYACETOPHENONE
- 2-HYDROXY-6-METHOXYACETOPHENONE
- 1-(2-HYDROXY-6-METHOXYPHENYL)ETHAN-1-ONE
- 1-(2-HYDROXY-6-METHOXYPHENYL)ETHANONE
- 2'-HYDROXY-6'-METHOXYACETOPHEN
- CAS:
- 703-23-1
- MF:
- C9H10O3
- MW:
- 166.17
- EINECS:
- 211-872-9
- Product Categories:
-
- Aromatic Acetophenones & Derivatives (substituted)
- Benzene series
- C9
- Carbonyl Compounds
- Ketones
- Mol File:
- 703-23-1.mol
2'-HYDROXY-6'-METHOXYACETOPHENONE Chemical Properties
- Melting point:
- 58-60 °C(lit.)
- Boiling point:
- 141 °C16 mm Hg(lit.)
- Density
- 1.158
- refractive index
- 1.5500 (estimate)
- Flash point:
- 141°C/16mm
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 9.79±0.10(Predicted)
- form
- solid
- color
- Light yellow to yellow
- BRN
- 1869049
- LogP
- 2.390 (est)
- CAS DataBase Reference
- 703-23-1(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2'-HYDROXY-6'-METHOXYACETOPHENONE Usage And Synthesis
Chemical Properties
Yellow crystalline powder
Uses
2''-Hydroxy-6''-methoxyacetophenone is useful in the synthesis of an aminopyrazole compound which is used to treat cancer and inhibits Chk1. 2''-Hydroxy-6''-methoxyacetophenone is also used to prepare 5,?4''-?disubstituted flavones, predicted androgen receptor antagonists and naphthopyrazolyl carbothioamides which are anticancer agents.
Uses
2′-Hydroxy-6′-methoxyacetophenone was used as starting material in the synthesis of 5-methoxyflavaone. It was also used in synthesis of 5,6-dihydroxyflavone.
Preparation
Preparation by reaction of methyl iodide on 2,6-dihydroxyacetophenone with potassium carbonate in boiling acetone (56%).
Definition
ChEBI: 2'-Hydroxy-6'-methoxyacetophenone is an aromatic ketone.
General Description
An organometallic synthetic route to 2′-hydroxy-6′-methoxyacetophenone was reported.
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