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Chemical Structure| 2199-87-3 Chemical Structure| 2199-87-3
Chemical Structure| 2199-87-3

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UBP608 is an effective negative allosteric modulator of the NMDA receptor (NMDAR), with potential for research into neurological diseases.

Synonyms: 6-Bromocoumarin-3-carboxylic acid

4.5 *For Research Use Only !

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Product Details of UBP608

CAS No. :2199-87-3
Formula : C10H5BrO4
M.W : 269.05
SMILES Code : O=C1OC2=C(C=C(Br)C=C2)C=C1C(O)=O
Synonyms :
6-Bromocoumarin-3-carboxylic acid
MDL No. :MFCD00047640
InChI Key :XFQHPAXNKDYMOX-UHFFFAOYSA-N
Pubchem ID :694463

Safety of UBP608

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313

Application In Synthesis of UBP608

* 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 [ 2199-87-3 ]

[ 2199-87-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 138907-68-3 ]
  • [ 2199-87-3 ]
  • ethyl 5-(6-bromo-2-oxo-2H-chromene-3-carboxamido)-1-(4-fluorophenyl)-1H-pyrazole-4-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
76% With pyridine; trichlorophosphate; General procedure: Intermediate 4 (0.001mol) and 5 (0.001mol) were dissolved in pyridine, phosphorus oxychloride is slowly added dropwise under ice bath conditions, then at 40-60C reacted for 5-8h. Finally, the mixture was poured into 30mL saturated Na2CO3 solution and stirred well. After the mixture was acidified, the saturated CuSO4 solution was used to remove pyridine, which greatly improved the purity and yield of the product. The data for compounds 8I-8VI are provided in the supporting information.
  • 2
  • [ 2199-87-3 ]
  • [ 15001-11-3 ]
  • ethyl 5-(6-bromo-2-oxo-2H-chromene-3-carboxamido)-1-(p-tolyl)-1H-pyrazole-4-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
81% With pyridine; trichlorophosphate; General procedure: Intermediate 4 (0.001mol) and 5 (0.001mol) were dissolved in pyridine, phosphorus oxychloride is slowly added dropwise under ice bath conditions, then at 40-60C reacted for 5-8h. Finally, the mixture was poured into 30mL saturated Na2CO3 solution and stirred well. After the mixture was acidified, the saturated CuSO4 solution was used to remove pyridine, which greatly improved the purity and yield of the product. The data for compounds 8I-8VI are provided in the supporting information.
  • 3
  • [ 2199-87-3 ]
  • [ 51516-70-2 ]
  • 6-bromo-N-(4-cyano-1-(4-fluorophenyl)-1H-pyrazol-5-yl)-2-oxo-2H-chromene-3-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With pyridine; trichlorophosphate; General procedure: Intermediate 4 (0.001mol) and 5 (0.001mol) were dissolved in pyridine, phosphorus oxychloride is slowly added dropwise under ice bath conditions, then at 40-60C reacted for 5-8h. Finally, the mixture was poured into 30mL saturated Na2CO3 solution and stirred well. After the mixture was acidified, the saturated CuSO4 solution was used to remove pyridine, which greatly improved the purity and yield of the product. The data for compounds 8I-8VI are provided in the supporting information.
  • 4
  • [ 2199-87-3 ]
  • [ 103646-82-8 ]
  • 6-bromo-N-(4-cyano-1-(p-tolyl)-1H-pyrazol-5-yl)-2-oxo-2H-chromene-3-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With pyridine; trichlorophosphate; General procedure: Intermediate 4 (0.001mol) and 5 (0.001mol) were dissolved in pyridine, phosphorus oxychloride is slowly added dropwise under ice bath conditions, then at 40?60°C reacted for 5?8h. Finally, the mixture was poured into 30mL saturated Na2CO3 solution and stirred well. After the mixture was acidified, the saturated CuSO4 solution was used to remove pyridine, which greatly improved the purity and yield of the product. The data for compounds 8I-8VI are provided in the supporting information.
 

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