Basic information Safety Supplier Related

5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI&

Basic information Safety Supplier Related

5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI& Basic information

Product Name:
5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI&
Synonyms:
  • 5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI&
  • 3-Isoxazolecarboxylicacid,5-cyclopropyl-(9CI)
  • 5-cyclopropylisoxazole-3-carboxylic acid(SALTDATA: FREE)
  • 3-Isoxazolecarboxylicacid, 5-cyclopropyl-
  • 5-cyclopropyl-3-isoxazolecarboxylic acid
CAS:
110256-15-0
MF:
C7H7NO3
MW:
153.14
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • OXAZOLE
  • GLYCINESCAFFOLD
  • CARBOXYLICACID
  • Building Blocks
  • Heterocyclic Building Blocks
  • Isoxazoles
Mol File:
110256-15-0.mol
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5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI& Chemical Properties

Melting point:
96-100 °C(lit.)
Boiling point:
358.1±30.0 °C(Predicted)
Density 
1.445
storage temp. 
Sealed in dry,Store in freezer, under -20°C
form 
solid
pka
3.46±0.10(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
HS Code 
2934999090
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5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI& Usage And Synthesis

Uses

5-Cyclopropylisoxazole-3-carboxylic Acid is a compound that has been used in the discovery, design and synthesis of a selective S1P3 receptor allosteric agonist (N,N-Dicyclohexyl-5-propylisoxazole-3-carboxamide).

Synthesis

21080-81-9

110256-15-0

The general procedure for the synthesis of 5-cyclopropylisoxazole-3-carboxylic acid from ethyl 5-cyclopropylisoxazole-3-carboxylate was as follows:Intermediate 16 - Preparation of 5-cyclopropylisoxazole-3-carboxylic acid. A mixture of ethyl 5-cyclopropylisoxazole-3-carboxylate (0.550 g, 3.04 mmol) with 1M aqueous sodium hydroxide (9.11 mL, 9.11 mmol) was stirred at room temperature for 72 hours. Upon completion of the reaction, the pH of the reaction solution was adjusted to 1 with 6N hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was separated, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give 0.446 g of 5-cyclopropylisoxazole-3-carboxylic acid as a solid in 96% yield. The product was confirmed by mass spectrometry: ESI/APCI(+) m/z: 154 (M+H), 176 (M+Na); ESI/APCI(-) m/z: 152 (M-H).

References

[1] Journal of Medicinal Chemistry, 2016, vol. 59, # 1, p. 358 - 373
[2] Patent: WO2010/142801, 2010, A1. Location in patent: Page/Page column 151
[3] Patent: US2003/236287, 2003, A1. Location in patent: Page 46, 47
[4] Patent: WO2016/40502, 2016, A1. Location in patent: Page/Page column 65
[5] Patent: WO2016/40504, 2016, A1. Location in patent: Paragraph 0194

5-CYCLOPROPYLISOXAZOLE-3-CARBOXYLIC ACI&Supplier

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