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Chemical Structure| 221300-34-1 Chemical Structure| 221300-34-1

Structure of 221300-34-1

Chemical Structure| 221300-34-1

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Product Details of [ 221300-34-1 ]

CAS No. :221300-34-1
Formula : C6H7FN2O2
M.W : 158.13
SMILES Code : O=C(C1=NNC=C1F)OCC
MDL No. :MFCD13175116

Safety of [ 221300-34-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 221300-34-1 ]

* 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 [ 221300-34-1 ]

[ 221300-34-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5932-27-4 ]
  • [ 221300-34-1 ]
YieldReaction ConditionsOperation in experiment
(a) 4-Fluoro<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong>The sub-title compound was prepared from <strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> in accordance with a literature procedure (R. Storer, et ah, Nucleosides Nucleotides 18, 203 (1999). A mixture (-2:1) of sub-title compound and unreacted starting material was obtained and used without further purification.
  • 2
  • [ 5932-27-4 ]
  • [ 221300-34-1 ]
  • [ 881668-91-3 ]
  • [ 1621-91-6 ]
YieldReaction ConditionsOperation in experiment
(b) 4-Fluoropyrazole-3-carboxylic acidSodium hydroxide (aq., 2M, 18 mmol; 9 mL) was added to a solution of a mixture (-2:1) of 4-fluoro<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> and <strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> (1.2 g, ~8 mmol; see step (a) above) in dioxane (9 mL) at rt and was stirred for 16 h. A second portion of aqueous sodium hydroxide (2M, 18 mmol, 9 mL) was added and the mixture was stirred for another 4 h. The mixture was acidified with HCl (aq., 2M, 20 mL), concentrated, stirred with MeOH (30 mL) and filtered. The filtrate was concentrated and the residue crystallised from HCl (aq., 0.01M)<to give a mixture (-3:1) of the sub-title compound and pyrazole- 3-carboxylic acid as a white solid (Yield: 267 mg (-2 mmol, ~25percent)). This mixture was employed without further purification.1H-NMR (DMSO-d6): delta 13.7-13.1 (br s, 1.3H), 7.9-7.7 (m, IH), 7.73 (d, 0.3H), 6.70 (d, 0.3H).
With sodium hydroxide; water; In 1,4-dioxane; at 20℃; for 20h; 4-Fluoropyrazole-3-carboxylic acid Aqueous NaOH (2M, 18 mmol, 9 mL) was added to a solution of a mixture (~2:1) of 4-fluoro<strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> and <strong>[5932-27-4]pyrazole-3-carboxylic acid ethyl ester</strong> (1.2 g, ~8 mmol; see step (a) above) in dioxane (9 mL) at room temperature and was stirred for 16 h. A second portion of aqueous NaOH (2M5 18 mmol, 9 mL) was added and the mixture was stirred for another 4 h. The mixture was acidified with aqueous HCl (2M, 20 mL), concentrated, stirred with MeOH (30 mL) and filtered. The filtrate was concentrated and the residue was crystallised with aqueous HCl (0.0 IM) to give a mixture (-3:1) of the sub-title compound and pyrazole-3-carboxylic acid as a white solid (Yield: 267 mg (~2 mmol, -25percent)). This mixture was employed without further purification. 1H-NMR (DMSO-d6): delta 13.7-13.1 (br s, 1.3H), 7.9-7.7 (m, IH), 7.73 (d, 0.3H), 6.70 (d, 0.3H)
 

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