| Identification | Back Directory | [Name]
Pyridine-3,5-dicarboxamide | [CAS]
4663-99-4 | [Synonyms]
3,5-Pyridinedicarboxamide Pyridine-3,5-dicarboxamide | [Molecular Formula]
C7H7N3O2 | [MDL Number]
MFCD00229426 | [MOL File]
4663-99-4.mol | [Molecular Weight]
165.15 |
| Chemical Properties | Back Directory | [Melting point ]
310-311 °C | [Boiling point ]
479.5±30.0 °C(Predicted) | [density ]
1.375±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
DMSO (Slightly) | [form ]
Solid | [pka]
14.08±0.50(Predicted) | [color ]
White to Pale Yellow |
| Hazard Information | Back Directory | [Synthesis]
The synthesis of pyridine-3,5-dicarboxamide was carried out according to Carelli's modified method. [38] Dichloromethane was used as a co-solvent to increase the reaction interface and to prevent foaming on addition of solids. Pyridine-3,5-dicarbonyl chloride (1.61 g, 7.89 mmol) was dissolved in dichloromethane (10 mL) with vigorous stirring at room temperature and the reaction was added slowly dropwise over a period of 1 hour. The reaction mixture was filtered through diatomaceous earth and subsequently recrystallized in ethanol/water (50:50) mixed solvent. Light yellow flaky crystals of pyridine-3,5-dicarboxamide (910 mg, 3.51 mmol, 70% yield) were obtained (Rf = 0, unfolding agent dichloromethane/methanol 10:1, melting point 115 °C). | [References]
[1] Journal of Organic Chemistry, 2015, vol. 80, # 5, p. 2676 - 2699 [2] Journal of the Chemical Society. Perkin Transactions 1, 2002, # 4, p. 542 - 547 [3] Synthesis (Germany), 2014, vol. 46, # 9, p. 1243 - 1253 [4] Monatshefte fuer Chemie, 1914, vol. 35, p. 783,784 [5] Monatshefte fuer Chemie, 1914, vol. 35, p. 783,784 |
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Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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