产品名称
3-氨基异噁唑, 95%
InChI
1S/C3H4N2O/c4-3-1-2-6-5-3/h1-2H,(H2,4,5)
SMILES string
Nc1ccon1
InChI key
RHFWLPWDOYJEAL-UHFFFAOYSA-N
assay
95%
form
liquid
refractive index
n20/D 1.511 (lit.)
bp
226-228 °C (lit.)
density
1.138 g/mL at 25 °C (lit.)
Quality Level
Application
3-Aminoisoxazole (isoxazol-3-amine) may be used in the following studies:
- As a reagent in the synthesis of N-(4-(N-isoxazol-3-ylsulfamoyl)phenyl)acetamide.
- As a starting material in the synthesis of N-(isoxazol-3-yl)-N′-(carbomethoxy)thiourea.
- As a starting material in the synthesis of (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxy-iminoacetic acid, a side-chain of the fourth generation of cephem antibiotics.
General description
3-Aminoisoxazole (isoxazol-3-amine) is a 3-substituted isoxazole derivative. It is a structural isomer of 5-aminoisoxazole.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F
flash_point_c
113 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Martin J. Walsh et al.
Probe Reports from the NIH Molecular Libraries Program, 2011 Oct 18 (Updated 2013 Feb 25) (2013-09-13)
The protist
Synthesis of 3-and 5-amino-5-(3)-(pyrrol-2-yl) isoxazoles.
Lyubov'N S, et al.
Tetrahedron, 61(20), 4841-4849 (2005)
Tomasz Glinka et al.
Bioorganic & medicinal chemistry, 11(4), 591-600 (2003-01-23)
SAR studies in a series of related 3-(heteroarylthio)cephems determined that a relatively high chemical reactivity of the beta-lactam ring, modulated by electronic effects of substituents at C-3 and C-7, is necessary to achieve high in vitro activity against methicillin-resistant Staphylococcus
Kuniaki Tatsuta
Proceedings of the Japan Academy. Series B, Physical and biological sciences, 84(4), 87-106 (2008-10-23)
The first total synthesis and development of a variety of bioactive natural products have been accomplished by using carbohydrates as a chiral source. In addition, practically useful intermediates have been created, analogs of natural products have been prepared, their structure-activity
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