5-AMINO-3-PHENYLISOXAZOLE
5-AMINO-3-PHENYLISOXAZOLE Basic information
- Product Name:
- 5-AMINO-3-PHENYLISOXAZOLE
- Synonyms:
-
- AKOS B029446
- 3-PHENYLISOXAZOLE-5-AMINE
- 3-PHENYLISOXAZOL-5-AMINE
- 3-PHENYL-ISOXAZOL-5-YLAMINE
- 3-PHENYL-5-ISOXAZOLAMINE
- 5-AMINO-3-PHENYLISOXAZOLE
- OTAVA-BB BB7020410006
- SALOR-INT L482897-1EA
- CAS:
- 4369-55-5
- MF:
- C9H8N2O
- MW:
- 160.17
- Product Categories:
-
- OXAZOLE
- Building Blocks
- Heterocyclic Building Blocks
- Isoxazoles
- Mol File:
- 4369-55-5.mol
5-AMINO-3-PHENYLISOXAZOLE Chemical Properties
- Melting point:
- 110-114 °C(lit.)
- Boiling point:
- 379.3±30.0 °C(Predicted)
- Density
- 1.204±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- solubility
- soluble in Methanol
- pka
- -1.69±0.10(Predicted)
- form
- Crystalline Powder
- color
- Orange
- CAS DataBase Reference
- 4369-55-5(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
5-AMINO-3-PHENYLISOXAZOLE Usage And Synthesis
Uses
3-Phenylon-5-aminoisoxazole is a heterocyclic organic compound that can be used as a pharmaceutical intermediate.
Chemical Properties
Yellow solid
Synthesis
614-16-4
4369-55-5
GENERAL METHOD: Benzoylacetonitrile (100 mmol) was added to 15% aqueous sodium hydroxide solution (100 mL) followed by hydroxylamine (200 mmol). The reaction mixture was heated to reflux for 14 h. After cooling to room temperature, the resulting precipitate was separated by filtration and recrystallized with isopropanol.
References
[1] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 6, p. 1914 - 1925
[2] Organic Letters, 2017, vol. 19, # 4, p. 934 - 937
[3] Organic Letters, 2018, vol. 20, # 9, p. 2774 - 2777
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 3, p. 1082 - 1105
[5] Patent: EP1813606, 2007, A1. Location in patent: Page/Page column 81
5-AMINO-3-PHENYLISOXAZOLE Preparation Products And Raw materials
Raw materials
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5-AMINO-3-PHENYLISOXAZOLE(4369-55-5)Related Product Information
- 3-(4-CHLOROPHENYL)ISOXAZOL-5-AMINE
- 5-AMINO-3-PHENYLISOXAZOLE
- 3-(4-METHYLPHENYL)ISOXAZOL-5-AMINE
- 3-(2-FLUORO-PHENYL)-ISOXAZOL-5-YLAMINE
- 5-AMINO-3-(4-FLUOROPHENYL)ISOXAZOLE
- 3-(4-NITRO-PHENYL)-ISOXAZOL-5-YLAMINE
- 2-Bromo-N-(3-phenyl-5-isoxazolyl)acetamide
- 3-Phenyl-N-(phenylmethylene)-5-isoxazolamine
- 5-AMINO-3-(4-METHOXYPHENYL)ISOXAZOLE
- 3-(4-METHOXYPHENYL)ISOXAZOL-5-AMINE
- 3-METHYL-4-PHENYL-5-ISOXAZOLAMINE
- 3-(4-BROMOPHENYL)ISOXAZOL-5-AMINE
- 3-M-TOLYL-ISOXAZOL-5-YLAMINE
- 3-METHYL-4-[3-(TRIFLUOROMETHYL)PHENYL]-5-ISOXAZOLAMINE
- 4-Morpholinepropanamine, beta-methyl-N-(3-phenyl-5-isoxazolyl)-
- 5-ANILINO-3-PHENYL-4-ISOXAZOLECARBALDEHYDE
- 1-Piperidinepropanamide, beta-methyl-N-(3-phenyl-5-isoxazolyl)-
- 1-Piperidineacetamide, N-(3-phenyl-5-isoxazolyl)-, monohydrochloride