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About This Item
Empirical Formula (Hill Notation):
C5H8N2O
CAS Number:
Molecular Weight:
112.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
form
solid
mp
118-122 °C (lit.)
SMILES string
Cc1noc(N)c1C
InChI
1S/C5H8N2O/c1-3-4(2)7-8-5(3)6/h6H2,1-2H3
InChI key
PYNDWPFZDQONDV-UHFFFAOYSA-N
General description
5-amino-3,4-dimethylisoxazole formed complexes with cobalt(II) and copper(II). The kinetics of gas-phase thermal isomerization of 5-amino-3,4-dimethylisoxazole was studied.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and characterization of cobalt (II) and copper (II) complexes with 5-amino-3, 4-dimethylisoxazole.
Biddau M, et al.
Transition Met. Chem. (London), 2(1), 5-9 (1977)
Gas-phase thermal isomerization of some aminomethylisoxazoles.
Perez JD, et al.
The Journal of Organic Chemistry, 46(17), 3505-3508 (1981)
S M Sicardi et al.
Mutation research, 343(1), 61-66 (1995-05-01)
Studies were undertaken to evaluate the ability of various quinoneimines to induce micronuclei in bone marrow cells as a measure of their genotoxicity. Accordingly, 2-hydroxy-N-(3,4-dimethyl-5-isoxazolyl)-1,4-naphthoquinone-4-imine (I), its 2-acetyl derivative (II) and 2-[(5-methyl-3-isoxazolyl)amino]-N-(5-methyl-3-isoxazolyl)-1 ,4- naphthoquinone-4-imine (III), as well as two of
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