3,5-Dimethyl-4-isoxazolamine

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CAS:31329-64-3
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3,5-Dimethyl-4-isoxazolamine manufacturers

3,5-Dimethyl-4-isoxazolamine Basic information
Product Name:3,5-Dimethyl-4-isoxazolamine
Synonyms:TIMTEC-BB SBB005896;AKOS B020738;3,5-DIMETHYL-4-ISOXAZOLAMINE;3,5-DIMETHYL-ISOXAZOL-4-YLAMINE;4-AMINO-3,5-DIMETHYLISOXAZOLE;ART-CHEM-BB B020738;3,5-dimethylisoxazol-4-amine;3,5-Dimethylisoxazole-4-amine
CAS:31329-64-3
MF:C5H8N2O
MW:112.13
EINECS:
Product Categories:Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Amines;Oxazoles, Isoxazoles & Benzoxazoles;Oxazole&Isoxazole;Oxazoles, Isoxazoles & Benzoxazoles;Building Blocks;Heterocyclic Building Blocks;Isoxazoles
Mol File:31329-64-3.mol
3,5-Dimethyl-4-isoxazolamine Structure
3,5-Dimethyl-4-isoxazolamine Chemical Properties
Melting point 41-46 °C(lit.)
Boiling point 78-80°C 0,4mm
density 1.118±0.06 g/cm3(Predicted)
storage temp. -20°C
form solid
pka1.59±0.10(Predicted)
AppearanceLight yellow to yellow Solid
InChI1S/C5H8N2O/c1-3-5(6)4(2)8-7-3/h6H2,1-2H3
InChIKeyINSUSOZBMWJGDG-UHFFFAOYSA-N
SMILESCc1noc(C)c1N
CAS DataBase Reference31329-64-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
HS Code 2934999090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
3,5-Dimethyl-4-isoxazolamine Usage And Synthesis
Uses4-Amino-3,5-dimethylisoxazole may be used in the synthesis of 3,5-dimethyl-4-phenylazoisoxazole via reaction with nitrosobenzene.The diazonium salt of 4-Amino-3,5-dimethylisoxazole can react with cupric sulfate to form acetyltriazole derivatives.
General Description4-Amino-3,5-dimethylisoxazole can be prepared via reduction of 3,5-dimethyl-4-nitroisoxazole in the presence of Zn/NH4Cl in H2O.
Synthesis
3,5-DIMETHYL-4-NITROISOXAZOLE

1123-49-5

3,5-Dimethyl-4-isoxazolamine

31329-64-3

Step A Synthesis of 3,5-dimethylisoxazol-4-amine: 12.00 g (84.44 mmol) of 3,5-dimethyl-4-nitroisoxazole was dissolved in 430 ml of water and 106.15 g (1.984 mol) of ammonium chloride was added. At 4°C, 46.93 g (7.17 mol) of zinc powder was added in batches over a period of 2 hours. Upon completion of the reaction, ethyl acetate was added to the reaction mixture for extraction and the organic phase was filtered through diatomaceous earth to remove solid impurities. The organic layer was dried with anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure to afford 3,5-dimethylisoxazol-4-amine in 86% (8.10 g) yield. The product was characterized by 1H-NMR (300 MHz, CDCl3): δ= 2.20 (s, 3H) ppm; 2.28 (s, 3H) ppm; 2.51 (wide s, 2H) ppm.

References[1] Helvetica Chimica Acta, 1991, vol. 74, # 3, p. 531 - 542
[2] Journal of the Chemical Society, 1921, vol. 119, p. 702
[3] Gazzetta Chimica Italiana, 1941, vol. 71, p. 327,336
[4] Patent: US2003/187028, 2003, A1
[5] Patent: US2002/82264, 2002, A1
3,5-Dimethyl-4-isoxazolamine Preparation Products And Raw materials
Raw materials3,5-DIMETHYL-4-NITROISOXAZOLE-->Ammonium chloride-->Ethyl acetate
Tag:3,5-Dimethyl-4-isoxazolamine(31329-64-3) Related Product Information
ISOXAFLUTOLE Isoxazole 3,5-Dimethylisoxazole Sulfamethoxazole Dimethyl phthalate Dimethyl sulfide Dimethyl fumarate Dimethyl ether Sulfisoxazole ETHANE N,N-Dimethyl-1,4-phenylenediamine Betaine Dimethyl sulfoxide Glycine N,N-Dimethylformamide Aminoethoxyvinyl glycine hydrochloride 3,5-DIMETHYLISOXAZOL-4-YL ISOCYANATE N,N'-BIS(5-METHYL-3-PHENYL-4-ISOXAZOLYL)UREA