2763-93-1

Basic information

• Product Name: 3-BROMO-5-AMINOMETHYLISOXAZOLE
• Synonyms: 5-AMINOMETHYL-3-BROMOISOXAZOLE;3-BROMO-5-AMINOMETHYLISOXAZOLE;(3-bromoisoxazol-5-yl)methylamine;(3-broMoisoxazol-5-yl)MethanaMine;(3-broMo-1,2-oxazol-5-yl)MethanaMine;5-Isoxazolemethanamine,3-bromo-
• CAS NO: 2763-93-1
• Molecular Formula: C4H5BrN2O
• Molecular Weight: 177
• Product Categories: Aminomethyl's;Oxazoles, Isoxazoles & Benzoxazoles;Oxazoles, Isoxazoles & Benzoxazoles
• Mol File: 2763-93-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 284.6 °C at 760 mmHg
• Flash Point: 125.9 °C
• Appearance: /
• Density: 1.741 g/cm³
• Vapor Pressure: 0.00296mmHg at 25°C
• Refractive Index: 1.558
• PKA: 7.33±0.29(Predicted)
• CAS DataBase Reference: 3-BROMO-5-AMINOMETHYLISOXAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMO-5-AMINOMETHYLISOXAZOLE(2763-93-1)
• EPA Substance Registry System: 3-BROMO-5-AMINOMETHYLISOXAZOLE(2763-93-1)

Safety Data

• Hazardous Substances Data: 2763-93-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H5BrN2O/c5-4-1-3(2-6)8-7-4/h1H,2,6H2

Upstream product

• 74213-24-4 N-dibromomethylidenehydroxylamine 
• 15430-52-1 prop-2-yn-1-amine hydrochloride 
• 124498-15-3 5-Chloromethyl-3-bromoisoxazole 
• 1203465-97-7 C₁₂H₇BrN₂O₃ 

Downstream Products

• 2763-94-2 5-aminomethyl-3-methoxyisoxazole 

Relevant articles and documents

Design, synthesis, and herbicidal activities of novel 2-cyanoacrylates containing isoxazole moieties

A series of novel 2-cyanoacrylates containing an isoxazole moiety were designed and synthesized. Their structures were characterized by 1H NMR and elemental analysis (or high-resolution mass spectrometry). Their herbicidal activities against four species were evaluated, and the results indicated that some of the title compounds showed excellent herbicidal activities against rape and amaranth pigweed in postemergence treatment even at a dose of 75 g/ha.

An improved synthesis of muscimol

A regiospecific 1,3-dipolar cycloaddition/elimination is the key-step of a convenient, gram-scale synthesis of the GABA-agonist muscimol (1).