838-34-6

Basic information

• Product Name: Benzoxazole, 2-(4-methoxyphenyl)-
• CAS NO: 838-34-6
• Molecular Formula: C14H11NO2
• Molecular Weight: 225.247
• Mol File: 838-34-6.mol
• Article Data: 228

Chemical Properties

• CAS DataBase Reference: Benzoxazole, 2-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoxazole, 2-(4-methoxyphenyl)-(838-34-6)
• EPA Substance Registry System: Benzoxazole, 2-(4-methoxyphenyl)-(838-34-6)

Safety Data

• Hazardous Substances Data: 838-34-6(Hazardous Substances Data)

Upstream product

• 3117-67-7 (E)-N-(4-methoxybenzylidene)-2-hydroxyaniline 
• 273-53-0 benzoxazole 
• 1950-68-1 4-methoxybenzenesulfonyl hydrazide 
• 98-68-0 4-methoxy-phenyl-sulphonyl chloride 
• 95-55-6 2-amino-phenol 
• 155164-68-4 4,5-Dichloro-2-(4-methoxy-benzoyl)-2H-pyridazin-3-one 
• 696-62-8 para-iodoanisole 
• 13939-06-5 molybdenum hexacarbonyl 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 123-11-5 4-methoxy-benzaldehyde 
• 615-36-1 2-bromoaniline 
• 615-43-0 2-iodophenylamine 
• 329939-01-7 N-(2-iodophenyl)-4-methoxybenzamide 
• 349614-89-7 N-(2-bromophenyl)-4-methoxybenzamide 

Downstream Products

• 3315-19-3 2-(4-hydroxyphenyl)benzoxazole 
• 1573171-23-9 C₂₀H₂₂BNO₄ 
• 1444302-88-8 2-(2-fluoro-4-methoxyphenyl)benzo[d]oxazole 

Relevant articles and documents

Synthesis, Characterization and DFT-D Studies of 2-Aminoethoxycalix[4]resorcinarenes: A Novel Heterogeneous Organocatalyst

The present article reports the synthesis of two novel supramolecular architectures, Phenyl(octa-2-aminoethoxy)calix[4]resorcinarene and 2-Aminoethoxyphenyl-(octa-2-aminoethoxy)calix[4]resorcinarene via surface functionalization and describes their applic

An efficient rapid synthesis of benzoxazoles and benzothiazoles using pma.Sio2 at room temperature under heterogeneous conditions

Treatment of 2-aminophenol (or 2-aminothiophenol) with aromatic aldehydes in the presence of phosphomolybdic acid on silica at room temperature affords the corresponding benzoxazoles (or benzothiazoles) in excellent yields (88-96%) under heterogeneous conditions. Benzoxazoles and benzothiazoles are formed in less than 10 min.

A TEMPO-Functionalized Ordered Mesoporous Polymer as a Highly Active and Reusable Organocatalyst

The properties of high stability, periodic porosity, and tunable nature of ordered mesoporous polymers make these materials ideal catalytic nanoreactors. However, their application in organocatalysis has been rarely explored. We report herein for the first time the incorporation of a versatile organocatalyst, 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO), into the pores of an FDU-type mesoporous polymer via a pore surface engineering strategy. The resulting FDU-15-TEMPO possesses a highly ordered mesoporous organic framework and enhanced stability, and shows excellent catalytic activity in the selective oxidation of alcohols and aerobic oxidative synthesis of 2-substituted benzoxazoles, benzimidazoles and benzothiazoles. Moreover, the catalyst can be easily recovered and reused for up to 7 consecutive cycles.