| Identification | Back Directory | [Name]
Benzo[d]isoxazol-5-ylaMine | [CAS]
239097-74-6 | [Synonyms]
1,2-benzoxazol-5-amine BENZO[D]ISOXAZOL-5-AMINE 1,2-benzisoxazol-5-amine 5-Aminobenzo[d]isoxazole 1,2-Benzoisoxazol-5-amine Benzo[d]isoxazol-5-ylaMine Benzo[d]isoxazol-5-ylamine(AK-64412) | [Molecular Formula]
C7H6N2O | [MDL Number]
MFCD13190363 | [MOL File]
239097-74-6.mol | [Molecular Weight]
134.14 |
| Chemical Properties | Back Directory | [Boiling point ]
311.6±15.0 °C(Predicted) | [density ]
1.317±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [pka]
2.67±0.10(Predicted) | [Appearance]
Light yellow to light brown Solid |
| Hazard Information | Back Directory | [Synthesis]
GENERAL STEPS: To a 12M HCl (0.5 mL) solution of SnCl4 (1.828 g, 7.02 mmol) under stirring was added 5-nitro-1,2-benzisoxazole (140 mg, 0.86 mmol) in a single addition at 0 °C. After a few minutes of reaction, a 12M HCl (0.5 mL) solution of SnCl2-2H2O (792 mg, 3.51 mmol) was added slowly and dropwise at 0 °C, followed by the addition of 12M HCl (1.0 mL). The reaction mixture was brought to room temperature and stirred continuously for 3 hours. Upon completion of the reaction, the reaction mixture was extracted with Et2O. The aqueous phase was adjusted to pH ~8 with saturated NaHCO3 solution and subsequently extracted with EtOAc. The organic phases were combined, dried with anhydrous Na2SO4, filtered and concentrated, and dried in vacuum to give 1,2-benzisoxazol-5-amine as a colorless solid (110 mg, 95% yield). The product was confirmed by 1H NMR (400 MHz, CDCl3): δ 8.54 (s, 1H), 7.42 (d, J=8.4 Hz, 1H), 6.94 (dd, J=8.4 Hz, 2.0 Hz, 1H), 6.91 (d, J=2.0 Hz, 1H). es-MS m/z: 135.1 [M+H]+. lc-MS analysis Shows purity of 90% (214 nm), retention time tR = 1.32 min. | [References]
[1] Patent: WO2016/73889, 2016, A1. Location in patent: Paragraph 00229 [2] Patent: WO2016/73895, 2016, A1. Location in patent: Paragraph 00286 [3] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 18, p. 6189 - 6196 |
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