1072-67-9 | 3-Amino-5-methylisoxazole

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$11.00	$8.00
10g	97%	in stock	$19.00	$14.00
25g	97%	in stock	$35.00	$25.00
100g	97%	in stock	$128.00	$90.00

Description

• Catalog Number: AB64272
• Chemical Name: 3-Amino-5-methylisoxazole
• CAS Number: 1072-67-9
• Molecular Formula: C4H6N2O
• Molecular Weight: 98.1032
• MDL Number: MFCD00003155
• SMILES: Nc1noc(c1)C
• NSC Number: 159134

Computed Properties

• Complexity: 66.7
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.1

Literature

• Catalytic ozonation of sulphamethoxazole in the presence of carbon materials: catalytic performance and reaction pathways.

  Journal of hazardous materials 20121115

• 4-{[(E)-2,3-Dihy-droxy-benzyl-idene]amino}-N-(5-methyl-1,2-oxazol-3-yl)benzene-sulfonamide.

  Acta crystallographica. Section E, Structure reports online 20120701

• Photo-removal of sulfamethoxazole (SMX) by photolytic and photocatalytic processes in a batch reactor under UV-C radiation (λmax=254 nm).

  Journal of hazardous materials 20110215

• Synthesis, antimicrobial, and mosquito larvicidal activity of 1-aryl-4-methyl-3,6-bis-(5-methylisoxazol-3-yl)-2-thioxo-2,3,6,10b-tetrahydro-1H-pyrimido[5,4-c]quinolin-5-ones.

  Bioorganic & medicinal chemistry letters 20101015

• Electrochemical abatement of the antibiotic sulfamethoxazole from water.

  Chemosphere 20101001

• Oxidation of sulfamethoxazole by UVA radiation and modified Fenton reagent: toxicity and biodegradability of by-products.

  Water science and technology : a journal of the International Association on Water Pollution Research 20090101

• Synthesis, potentiometric and antimicrobial studies on metal complexes of isoxazole Schiff bases.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20080601

• (E)-2-Meth-oxy-6-[(5-methyl-isoxazol-3-yl)imino-meth-yl]phenol.

  Acta crystallographica. Section E, Structure reports online 20080201

• Transformation of the antibacterial agent sulfamethoxazole in reactions with chlorine: kinetics, mechanisms, and pathways.

  Environmental science & technology 20041101