415715-07-0

Basic information

• Product Name: 4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
• Synonyms: 4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol
• CAS NO: 415715-07-0
• Molecular Weight: 232.239
• Mol File: 415715-07-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol(415715-07-0)
• EPA Substance Registry System: 4-methoxy-2-[(5-methyl-3-isoxazolyl)imino]methylphenol(415715-07-0)

Safety Data

• Hazardous Substances Data: 415715-07-0(Hazardous Substances Data)

Upstream product

• 1072-67-9 5-methylisoxazol-3-ylamine 
• 672-13-9 2-hydroxy-5-methoxybenzaldehyde 

Downstream Products

• 1153622-45-7 4-methoxy-2-[(5-methyl-3-isoxazolyl)amino]methylphenol 
• 1233715-12-2 C₂₀H₁₉N₃O₄ 
• 1233714-98-1 C₁₉H₁₉N₃O₄ 

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

A simple method for the synthesis of 5-isoxazolyl-4-thioxo-1,3,5- benzoxadiazocines

Synthesis of novel isoxazolyl 1,3,5-benzoxadiazocines 5 has been accomplished by condensation of 3-amino-5-methylisoxazole 1 with salicylaldehydes, followed by reduction, treatment with arylisothio-cyanates, and subsequent ring closure in the presence of