13676-48-7

Basic information

• Product Name: 5-Amino-2-(3-aminophenyl)benzoxazole
• Synonyms: 5-Amino-2-(3-aminophenyl)benzoxazole;5-Amino-2-(m-aminophenyl)benzoxazole
• CAS NO: 13676-48-7
• Molecular Formula: C₁₃H₁₁N₃O
• Molecular Weight: 225.25
• Product Categories: Chemical Amines;Amines;Aromatics;Heterocycles
• Mol File: 13676-48-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 450 °C at 760 mmHg
• Flash Point: 225.9 °C
• Appearance: /
• Density: 1.329 g/cm³
• Vapor Pressure: 2.74E-08mmHg at 25°C
• Refractive Index: 1.729
• CAS DataBase Reference: 5-Amino-2-(3-aminophenyl)benzoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Amino-2-(3-aminophenyl)benzoxazole(13676-48-7)
• EPA Substance Registry System: 5-Amino-2-(3-aminophenyl)benzoxazole(13676-48-7)

Safety Data

• Hazardous Substances Data: 13676-48-7(Hazardous Substances Data)

Usage

General Description

5-Amino-2-(3-aminophenyl)benzoxazole is a chemical compound with the molecular formula C13H11N3O. It is a benzoxazole derivative, which means it contains a benzene ring fused to an oxazole ring. 5-Amino-2-(3-aminophenyl)benzoxazole has two amino groups and one substituted phenyl group. It is a heterocyclic compound that has potential applications in the pharmaceutical industry, such as in the development of drugs with biological activity. Its structure and properties make it of interest for further study as a potential component in drug discovery and development.

InChI:InChI=1/C13H11N3O/c14-9-3-1-2-8(6-9)13-16-11-7-10(15)4-5-12(11)17-13/h1-7H,14-15H2

Upstream product

• 137-09-7 2,4-diaminophenol dihydrochloride 
• 99-05-8 meta-aminobenzoic acid 
• 99-57-0 2-hydroxy-5-nitroaniline 
• 121-90-4 m-nitrobenzoic acid chloride 
• 105753-07-9 C₁₃H₉N₃O₆ 

Downstream Products

• 1033093-54-7 C₃₁H₄₅N₅O₃ 

Relevant articles and documents

Effect of isomerism on molecular packing and gas transport properties of poly(benzoxazole-co-imide)s

A facile approach to synthesize poly(benzoxazole-co-imide)s without thermal rearrangement at high temperature is proposed. Poly(benzoxazole-co-imide)s with improved mechanical and solution-processable properties were prepared through polycondensation of 4

Gelation-induced fluorescence enhancement of benzoxazole-based organogel and its naked-eye fluoride detection

The benzoxazole derivative gelator 1 forms a stable DMF/toluene cosolvent gel with dramatically enhanced fluorescence emission compared to its mother solution. The translucent colorless gel was changed to a solution with strong greenish fluorescence in th

Process for making 2-aryl benz (ox, thi, imid)azoles and 2-aminoaryl aminobenz(ox, thi, imid)azoles

2-(aryl)-benz(ox, thi, imid)azoles are prepared by reacting an aromatic aldehyde with hydroxylamine to form an aromatic aldehyde oxime, halogenating the oxime to form an aromatic hydroxamoyl halide, and then reacting this halide with certain aromatic amine compounds. The products may be nitrated and then reduced to form the corresponding diamines, which are useful in making PIBX polymers.