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经验公式(希尔记法):
C4H6N2O
化学文摘社编号:
分子量:
98.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
238-719-9
MDL number:
产品名称
5-氨基-3-甲基异噁唑, 98%
assay
98%
InChI key
FNXYWHTZDAVRTB-UHFFFAOYSA-N
InChI
1S/C4H6N2O/c1-3-2-4(5)7-6-3/h2H,5H2,1H3
SMILES string
Cc1cc(N)on1
mp
85-87 °C (lit.)
General description
5-氨基-3-甲基异噁唑可与α,β-不饱和酮反应形成相应的异噁唑[5,4-b]吡啶。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Wafaa S Hamama et al.
Archiv der Pharmazie, 345(6), 468-475 (2012-03-03)
The reaction of 5-amino-3-methylisoxazole with appropriate α,β-unsaturated ketones gave the corresponding isoxazolo[5,4-b]pyridines. Treatment of 1 with 2,6-dibenzylidenecyclohexanone or 2-benzylidenedimedone afforded the corresponding isoxazolo[5,4-b]quinoline derivatives. 4,6,8,9-Tetrahydroisoxazolo[5,4-b]quinolin-5-one derivative was also obtained by multicomponent condensation reaction of 1 with dimedone and benzaldehyde. Heterocyclic
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