1396795-65-5

Basic information

• Product Name: tert-butyl (2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetate
• Synonyms: tert-butyl (2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetate
• CAS NO: 1396795-65-5
• Molecular Weight: 325.364
• Mol File: 1396795-65-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: tert-butyl (2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetate(1396795-65-5)
• EPA Substance Registry System: tert-butyl (2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetate(1396795-65-5)

Safety Data

• Hazardous Substances Data: 1396795-65-5(Hazardous Substances Data)

Upstream product

• 863724-27-0 tert-butyl (5-bromo-2-oxo-1,3-benzoxazol-3(2H)-yl)acetate 
• 14733-73-4 5-bromo-1,3-benzoxazol-2(3H)-one 
• 108-86-1 bromobenzene 
• 863724-59-8 tert-butyl [2-oxo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzoxazol-3(2H)-yl]acetate 
• 40925-68-6 2-amino-4-bromo-phenol 
• 7693-52-9 4-bromo-2-nitrophenol 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 1226180-82-0 5-phenyl-1,3-benzoxazol-2(3H)-one 

Downstream Products

• 863724-28-1 (2-Oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetic acid 
• 1396795-69-9 N-methyl-2-(2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)-N-(pyridin-4-yl)acetamide 
• 1396795-70-2 N-[2-(bromomethyl)phenyl]-N-methyl-2-(2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetamide 
• 1396795-71-3 N-[3-(bromomethyl)phenyl]-N-methyl-2-(2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetamide 
• 1396795-78-0 C₂₂H₂₀N₂O₂ 
• 1396795-73-5 C₂₅H₂₅N₃O₃ 
• 1396795-72-4 N-[4-(bromomethyl)phenyl]-N-methyl-2-(2-oxo-5-phenyl-1,3-benzoxazol-3(2H)-yl)acetamide 

Relevant articles and documents

Convenient synthesis of benzoxazolone derivatives by cross-coupling of benzoxazolone boronates with aryl halides

Benzoxazolone derivatives with various substituents at the C-5 position were synthesized efficiently via benzoxazolone boronates as the key intermediate. The target compounds were also synthesized from (het)aryl halides in a one-pot process. These methods permitted efficient exploratory syntheses of a series of benzoxazolone derivatives. Georg Thieme Verlag Stuttgart New York.