112633-37-1

Basic information

• Product Name: 3-Isoxazolamine, 5-methyl-N-(phenylmethylene)-
• CAS NO: 112633-37-1
• Molecular Formula: C11H10N2O
• Molecular Weight: 186.213
• Mol File: 112633-37-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-Isoxazolamine, 5-methyl-N-(phenylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Isoxazolamine, 5-methyl-N-(phenylmethylene)-(112633-37-1)
• EPA Substance Registry System: 3-Isoxazolamine, 5-methyl-N-(phenylmethylene)-(112633-37-1)

Safety Data

• Hazardous Substances Data: 112633-37-1(Hazardous Substances Data)

Usage

Structure

Contains a five-membered heterocyclic ring (isoxazole) with oxygen and nitrogen atoms. Also includes a methyl group and a phenylmethylene group.

Properties

Specific properties such as melting point, boiling point, solubility, and reactivity would require experimental data or computational analysis for accurate determination.

Applications

Potential uses in medicinal chemistry, agricultural chemistry, and organic synthesis.

Research Needs

Further investigation and analysis are necessary to uncover its full range of potential uses and effects.

Upstream product

• 1072-67-9 5-methylisoxazol-3-ylamine 
• 100-52-7 benzaldehyde 

Downstream Products

• 119485-39-1 2-(5-Methyl-isoxazol-3-yl)-1,3-diphenyl-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazine 
• 119485-30-2 1-[(5-methyl-isoxazol-3-ylamino)-phenyl-methyl]-naphthalen-2-ol 
• 1428968-09-5 1-(1H-indol-3-yl)-2-((5-methylisoxazol-3-yl)amino)-2-phenylethanone 
• 1206182-22-0 5-(6-methoxynaphthalen-2-yl)-1-(5-methylisoxazol-3-ylamino)-1-phenylpentan-3-one 
• 1295478-30-6 C₂₀H₁₈N₄O₂S 
• 1295478-29-3 C₁₉H₁₅ClN₄O₂S 
• 1295478-26-0 C₂₀H₁₈N₄O₃S 
• 1295478-17-9 C₁₉H₁₆N₄O₂S 
• 1295478-04-4 C₁₂H₁₁N₃OS 

Relevant articles and documents

Isoxazole derivatives as potent transient receptor potential melastatin type 8 (TRPM8) agonists

Modulation of the transient receptor potential melastatin type-8 (TRPM8), the receptor for menthol acting as the major sensor for peripheral innocuous cool temperatures, has several important applications in pharmaceutical, food and cosmetic industries. I

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