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Product Name:
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4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]benzoic acid |
| Synonyms: |
4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]benzoicacid;NilotinibEPImpurityD; 4-Methyl-3-{[4-(pyridin-3-yl)pyrimidin-2-yl]amino}benzoicacid;Benzoicacid; 4-Methyl-3-[[4-(3-pyridinyl)-2-pyriMidinyl]aMino]-; 4-Methyl-3-[[4-(3-pyridinyl)-2-pyriMidiny]aMino]benzoicacid; 2-[(5-Carboxy-2-methylphenyl)amino]-4-(pyridin-3-yl)pyrimidine; 3-{2-[(5-Carboxy-2-methylphenyl)amino]pyrimidin-4-yl}pyridine; NilotinibIntemediate2; |
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CAS:
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641569-94-0 |
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MF:
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C17H14N4O2 |
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MW:
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306.32 |
| EINECS: | 629-968-8 |
| Boiling Point | 587.9±60.0 °C(Predicted) |
| Melting Point | >257oC (dec.) |
| Density | 1.336 |
| Acidity Coefficient (pKa) | 4.35±0.10(Predicted) |
| Solubility | Soluble in DMSO (slightly), methanol (slightly, with heating) |
| Form | Solid |
| Color | Light beige |
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Storage temp.
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under inert gas (nitrogen or Argon) at 2–8 °C |
Usage
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Uses
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It is a key intermediate in the synthesis of nilotinib (an antineoplastic drug) and plays an important role in the preparation of nilotinib. Its structural carboxyl group can be converted to an acyl chloride under the action of thionyl chloride, laying a foundation for subsequent chemical transformations. The generated acyl chloride can be further converted to an ester group, facilitating the structural construction of relevant drug molecules or derivatives. |
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