101097-11-4

Basic information

• Product Name: Benzoxazole, 2-(2-Methoxyphenyl)-5-Methyl-
• Synonyms: Benzoxazole, 2-(2-Methoxyphenyl)-5-Methyl-;2-(2-Methoxyphenyl)-5-Methylbenzo[d]oxazole
• CAS NO: 101097-11-4
• Molecular Formula: C₁₅H₁₃NO₂
• Molecular Weight: 239.26922
• Mol File: 101097-11-4.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoxazole, 2-(2-Methoxyphenyl)-5-Methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoxazole, 2-(2-Methoxyphenyl)-5-Methyl-(101097-11-4)
• EPA Substance Registry System: Benzoxazole, 2-(2-Methoxyphenyl)-5-Methyl-(101097-11-4)

Safety Data

• Hazardous Substances Data: 101097-11-4(Hazardous Substances Data)

Upstream product

• 135-02-4 ortho-anisaldehyde 
• 95-84-1 3-amino-4-hydroxytoluene 
• 10531-78-9 5-methyl-1,3-benzoxazole 
• 6609-56-9 2-methoxy-benzonitrile 
• 766-51-8 2-Chloroanisole 
• 22538-72-3 2-(2-Methoxy-benzylidenamino)-4-methylphenol 
• 6850-57-3 2-methoxybenzylamine 

Relevant articles and documents

Palladium(II) Immobilized Onto the Glucose Functionalized Magnetic Nanoparticle as a New and Efficient Catalyst for the One-pot Synthesis of Benzoxazoles

Palladium(II) have been immobilized into the nano magnetic Fe3O4 which was functionalized with glucose in order to achieve a one-pot synthesis of 2-substituted benzoxazole derivatives with high yields in the diverse range of organic solvents. The nano catalyst is highly dispersive in polar solvents and can be easily recovered and reused for 6 runs without significant loss of its activity. Finally, the catalyst was fully characterized by FT-IR, TGA, CHN, SEM, EDX and atomic absorption spectroscopy.

N-Heterocyclic Carbene (NHC)-Catalyzed One-Pot Aerobic Oxidative Synthesis of 2-Substituted Benzo[ d ]oxazoles, Benzo[ d ]thiazoles and 1,2-Disubstituted Benzo[ d ]imidazoles

N-Heterocyclic carbene (NHC), generated in situ from easily available N-heterocyclic imidazolium salt with air as terminal oxidant, has successfully been utilized as a cheap and efficient catalyst for one-pot aerobic oxidative synthesis of 2-arylbenzo[ d ]oxazoles, 2-substituted benzo[ d ]thiazoles, and 1,2-disubstituted benzo[ d ]imidazoles.

Nickel-Catalyzed Coupling of Azoles with Aromatic Nitriles

This manuscript describes the Ni-catalyzed coupling of azoles with aromatic nitriles. The use of BPh3 promotes these arylations with electronically diverse azoles and benzonitriles. While the nickel catalyst is necessary for the arylations of phenyl oxazoles, arylation of benzoxazoles with some nitriles affords the arylated products even in the absence of the Ni catalyst albeit in lower yield than the catalyzed process. The Ni-catalyzed process exhibits higher rates and a broader scope than the uncatalyzed transformation.