2-Hydroxy-4-methylquinoline
Based on 1 Customer Validation
2-Hydroxy-4-methylquinoline is a synthetic intermediate. 2-Hydroxy-4-methylquinoline is formed via cyclization of acetoacetanilide under the action of concentrated sulfuric acid through the Conrad-Limpach-Knorr synthesis. 2-Hydroxy-4-methylquinoline can be used in studies related to the synthesis of chemotherapeutic agents.
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- CAS No.: 607-66-9
- Formule: C10H9NO
- Masse moléculaire:159.19
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Stockage:
Store at room temperature 3 years.
In solvent -80°C, 2 years , -20°C, 1 year
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Activité biologique
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Chemical Information
- Pureté et documentation
- Références
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Help & FAQs
Activité biologique
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| LNCaP | IC50 |
125.7 μM
Compound: 1c
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Cytotoxicity against human LNCAP cells after 72 hrs by sulforhodamine B assay
Cytotoxicity against human LNCAP cells after 72 hrs by sulforhodamine B assay
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[PMID: 19265439] |
Chemical Information
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CAS No. 607-66-9
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Appearance Solid
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Masse moléculaire 159.19
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Formule C10H9NO
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SMILES
O=C1C=C(C=2C=CC=CC2N1)C
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Store at room temperature 3 years
In solvent -80°C 2 years -20°C 1 year
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
2-Hydroxy-4-methylquinoline Related Classifications
HY-W106109 Related Classifications
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