1373758-48-5

Basic information

• Product Name: 5-(4-ethoxyphenyl)-2-phenyloxazole
• Synonyms: 5-(4-ethoxyphenyl)-2-phenyloxazole
• CAS NO: 1373758-48-5
• Molecular Weight: 265.312
• Mol File: 1373758-48-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 5-(4-ethoxyphenyl)-2-phenyloxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-ethoxyphenyl)-2-phenyloxazole(1373758-48-5)
• EPA Substance Registry System: 5-(4-ethoxyphenyl)-2-phenyloxazole(1373758-48-5)

Safety Data

• Hazardous Substances Data: 1373758-48-5(Hazardous Substances Data)

Upstream product

• 2835-06-5 phenylglycin 
• 79887-14-2 4-ethoxyphenylacetylene 
• 1676-63-7 4'-ethoxyacetophenone 
• 100-46-9 benzylamine 
• 433229-42-6 2-(4-methoxyphenyl)acetaldehyde 
• 19226-36-9 3-phenyl-5H-1,4,2-dioxazol-5-one 

Relevant articles and documents

Synthesis of 2,5-Disubstituted Oxazoles from Arylacetylenes and α-Amino Acids through an i 2 /Cu(NO 3) 2 ?3H 2 O-Assisted Domino Sequence

A new strategy has been developed for the synthesis of 2,5-disubstituted oxazoles from easily available arylacetylenes and α-amino acids in the presence of Cu(NO 3) 2 ?3H 2 O and iodine. This reaction process involves the I 2 /Cu(NO 3) 2 ?3H 2 O-assisted transformation of arylacetylene to α-iodo acetophenone, Kornblum oxidation to phenylglyoxal, condensation to imine, decarboxylation/annulation/oxidation reaction sequence to approach 2,5-disubstituted oxazoles.

Synthesis of oxazoles through copper-mediated aerobic oxidative dehydrogenative annulation and oxygenation of aldehydes and amines

A fragment-assembling strategy is used to form oxazoles from aryl acetaldehydes, amines, and molecular oxygen under mild conditions (see scheme). The transformation is highly efficient with the removal of six hydrogen atoms, including the cleavage of four C(sp3)-H bonds. Copyright