112633-43-9

Basic information

• Product Name: Phenol, 2-[[(5-methyl-3-isoxazolyl)imino]methyl]-
• CAS NO: 112633-43-9
• Molecular Formula: C11H10N2O2
• Molecular Weight: 202.213
• Mol File: 112633-43-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[[(5-methyl-3-isoxazolyl)imino]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[[(5-methyl-3-isoxazolyl)imino]methyl]-(112633-43-9)
• EPA Substance Registry System: Phenol, 2-[[(5-methyl-3-isoxazolyl)imino]methyl]-(112633-43-9)

Safety Data

• Hazardous Substances Data: 112633-43-9(Hazardous Substances Data)

Upstream product

• 1072-67-9 5-methylisoxazol-3-ylamine 
• 89-95-2 2-methyl-benzyl alcohol 
• 90-02-8 salicylaldehyde 

Downstream Products

• 298216-14-5 2-[(5-methyl-3-isoxazolyl)amino]methylphenol 
• 1233715-20-2 C₁₉H₁₆ClN₃O₃ 
• 1233715-19-9 C₁₉H₁₆BrN₃O₃ 
• 1233715-18-8 C₂₀H₁₉N₃O₄ 
• 1233715-17-7 C₂₀H₁₉N₃O₃ 
• 1233715-10-0 C₁₉H₁₇N₃O₃ 
• 1233715-06-4 C₁₈H₁₆ClN₃O₃ 
• 1233715-05-3 C₁₈H₁₆BrN₃O₃ 
• 1233715-04-2 C₁₉H₁₉N₃O₄ 
• 1233715-03-1 C₁₉H₁₉N₃O₃ 
• 1233714-96-9 N₂-(2-hydroxybenzyl)-N₂-(5-methyl-3-isoxazolyl)-N₁-phenylurea 
• 119485-44-8 C₂₈H₂₂N₂O₄ 

Relevant articles and documents

Unusual products of reaction between aminoisoxazoles and aromatic aldehydes

The reaction between primary amine and aldehyde usually leads to a Schiff base. In this work, we present the results of research (NMR, ATR-FTIR, UV–Vis, and X-ray) of products obtained in the reaction of 5-methyl-3-aminoisoxazole (3AMI) or 3-methyl-5-amin

Synthesis of novel isoxazolyl 3,4,5,6-tetrahydro-2H-1,3,5-benzoxadiazocin- 4-ones as possible biodynamic agents

Synthesis of new isoxazolyl 1,3,5-benzoxadiazocin-4-ones 5 has been accomplished by condensation of 3-amino-5-methylisoxazole 1 with salicylaldehydes, followed by reduction, treatment with arylisocyanates and subsequent ring closure in presence of formald

Solvent-free syntheses of salicylaldimines assisted by microwave irradiation

A microwave-assisted condensation of salicylaldehyde and aryl amines without solvent were efficiently performed to form a series of salicylaldimines in high yields, which were confirmed by IR, 1H NMR, 13C NMR and elemental analyses. The microwave-assisted condensation provided a convenient environmental-friendship methodology for syntheses of Schiff-base in organic syntheses.