112633-38-2

Basic information

• Product Name: 3-Isoxazolamine, 5-methyl-N-[(4-methylphenyl)methylene]-
• CAS NO: 112633-38-2
• Molecular Formula: C12H12N2O
• Molecular Weight: 200.24
• Mol File: 112633-38-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Isoxazolamine, 5-methyl-N-[(4-methylphenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Isoxazolamine, 5-methyl-N-[(4-methylphenyl)methylene]-(112633-38-2)
• EPA Substance Registry System: 3-Isoxazolamine, 5-methyl-N-[(4-methylphenyl)methylene]-(112633-38-2)

Safety Data

• Hazardous Substances Data: 112633-38-2(Hazardous Substances Data)

Usage

Chemical compound

3-Isoxazolamine, 5-methyl-N-[(4-methylphenyl)methylene]-

Class

Isoxazoles

Molecular weight

187.24 g/mol

Physical state

Yellow to brown solid

Structural features

Five-membered ring with oxygen and nitrogen atoms, methyl group, substituted phenylmethylene group

Potential applications

Pharmaceutical and agrochemical industries due to unique structure and potential biological activity

Upstream product

• 1072-67-9 5-methylisoxazol-3-ylamine 
• 104-87-0 4-methyl-benzaldehyde 

Downstream Products

• 1315257-54-5 N-(4-methylbenzyl)-N-(5-methyl-3-isoxazolyl)amine 
• 1295478-32-8 C₂₀H₁₇BrN₄O₂S 
• 1295478-20-4 C₂₀H₁₈N₄O₂S 
• 1295478-09-9 C₁₃H₁₃N₃OS 
• 119485-33-5 1-[(5-methyl-isoxazol-3-ylamino)-p-tolylmethyl]-naphthalen-2-ol 
• 119485-42-6 2-(5-Methyl-isoxazol-3-yl)-1,3-di-p-tolyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine 
• 1190945-12-0 5-(6-methoxynaphthalen-2-yl)-1-(5-methylisoxazol-3-ylamino)-1-(p-tolyl)pentan-3-one 

Relevant articles and documents

Synthesis and antidiabetic performance of β-amino ketone containing nabumetone moiety

We wish to report the further design and improved synthesis that resulted in two series of target molecules, TM-1 and TM-2, with remarkably simplified structures containing β-amino ketone of discrete nabumetone moiety. These were obtained via a 'one-pot,

Synthesis of isoxazolyl oxadiazolines and thiazolidinones

4-(5-Methyl-3-isoxazolyl)-3,5-diaryl-Δ2-1,2,4-oxadiazolines have been prepared by benzonitrile oxide addition to 3-benzalamino-5-methyl isoxazoles. The Schiff bases have been obtained by the condensation of aromatic aldehydes with 3-amino-5-met