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Chemical Structure| 1452-63-7 Chemical Structure| 1452-63-7
Chemical Structure| 1452-63-7

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Synonyms: 2-Pyridinecarbohydrazide

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Product Details of 2-Pyridinecarbohydrazide

CAS No. :1452-63-7
Formula : C6H7N3O
M.W : 137.14
SMILES Code : O=C(NN)C1=NC=CC=C1
Synonyms :
2-Pyridinecarbohydrazide
MDL No. :MFCD00059782
InChI Key :BAQLNPIEFOYKNB-UHFFFAOYSA-N
Pubchem ID :255881

Safety of 2-Pyridinecarbohydrazide

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P280-P305+P351+P338-P310

Application In Synthesis of 2-Pyridinecarbohydrazide

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1452-63-7 ]

[ 1452-63-7 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 1452-63-7 ]
  • [ 103854-64-4 ]
  • C17H14N4O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
74% In ethanol; for 1h;Reflux; Compound 2 (200 mg, 1.156 mmol) and picolinohydrazide (3) (190 mg, 1.387 mmol) were dissolved in 25 mL of absolute ethanol, the solution was heated to reflux and stirred for 1 h. After cooled to room temperature, the pale yellow precipitates formed was collected by filtration, which was washed with ethanol and dried under vacuum to give 1 in 74% yield. mp 182.5-183 C. 1H NMR (400 MHz, DMSO-d6) δ 12.69 (s, 1H), 8.77 (s, 1H), 8.72 (d,1H, J = 4.4 Hz), 8.33 (d, 1H, J = 4.8 Hz), 8.13 (t, 2H, J = 9.2Hz), 8.05 (t, 1H, J = 7.2 Hz), 7.67 (dd, 1H, J1 = 6.8 Hz, J2 =5.2 H), 7.54-7.48 (m, 2H), 7.20 (d, 1H, J = 6.8 Hz), 3.96 (s,3H). 13C NMR (100 MHz, DMSO-d6) δ 161.35, 155.58, 152.93, 149.78, 149.52, 149.02, 139.51, 138.55, 136.93, 129.40, 128.26, 127.67, 123.45, 119.82, 118.37, 109.36,56.02. HRMS (ESI+) cacld for C17H14N4O2Na: 329.1014, found: m/z 329.1017 [M+Na]+.
  • 3
  • [ 1452-63-7 ]
  • [ 87220-68-6 ]
  • 2-(9-phenyl-9H-carbazole-3-yl)-5-(pyridin-2-yl)-1,3,4-oxadiazole [ No CAS ]
YieldReaction ConditionsOperation in experiment
39.9% In ethanol;Reflux; 9-Phenyl-9H-carbazole-3-carbaldehyde (2.71 g, 10 mmol) was added to the reaction flask and2-pyridinecarboxylic acid hydrazide (1.37 g, 10 mmol) followed by 120 mL of ethanol,The reaction was heated and stirred at reflux overnight. After cooling to room temperature,Slowly pour the reaction mixture into 500 mL of deionized water, and let it stand for 2 minutes after stirring for 10 minutes.Filter off and collect the white solid. The resulting white cake is in turn deionized water andEthanol was washed and placed in a vacuum oven at 50C for 24 hours.The dried intermediate product was placed in a single-mouth reaction flask and 70 mL of acetonitrile was added sequentially.30mL 1,4-dioxane and 150mL sodium hypochlorite solution,Stir for 30 min at room temperature. Pour the reaction slowly into 500mLDeionized water and extracted with dichloromethane (150 mL x 3).The organic phases were combined and washed with deionized water (200 mL x 3).The resulting organic phase was dried over anhydrous magnesium sulfate and concentrated.Column chromatography using ethyl acetate and petroleum ether as eluents gives the product L3 as a white solid.(1.55 g, 3.99 mmol), yield 39.9%.
  • 4
  • [ 1452-63-7 ]
  • [ 7113-10-2 ]
  • 2-phenyl-N′-picolinoylthiazole-4-carbohydrazide [ No CAS ]
  • 5
  • [ 1452-63-7 ]
  • [ 39067-29-3 ]
  • N′-picolinoyl-2-(pyridin-3-yl)thiazole-4-carbohydrazide [ No CAS ]
 

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