1011269-40-1

Basic information

• Product Name: 5-cyclohex-1-enyl-3-phenyl-3H-oxazol-2-one
• Synonyms: 5-cyclohex-1-enyl-3-phenyl-3H-oxazol-2-one
• CAS NO: 1011269-40-1
• Molecular Weight: 241.29
• Mol File: 1011269-40-1.mol

Chemical Properties

• CAS DataBase Reference: 5-cyclohex-1-enyl-3-phenyl-3H-oxazol-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-cyclohex-1-enyl-3-phenyl-3H-oxazol-2-one(1011269-40-1)
• EPA Substance Registry System: 5-cyclohex-1-enyl-3-phenyl-3H-oxazol-2-one(1011269-40-1)

Safety Data

• Hazardous Substances Data: 1011269-40-1(Hazardous Substances Data)

Upstream product

• 3422-02-4 N-(benzyloxycarbonyl)aniline 
• 21983-34-6 1-(bromoethynyl)cyclohex-1-ene 
• 1011269-23-0 cyclohex-1-enylethynyl-phenyl-carbamic acid tert-butyl ester 

Relevant articles and documents

Zinc Chloride Mediated Synthesis of 3H-Oxazol-2-one and Pyrrolo-oxazin-1-one from Ynamide

A simple zinc chloride mediated cyclization of ynamidyl N-carbamates or 2-ynamidyl-(hetero)arylcarboxylates is achieved under mild reaction conditions, leading to the synthesis of useful heterocyclic scaffolds, 3H-oxazol-2-ones and pyrrolo-oxazin-1-ones, with good yields.

An efficient silver tetrafluoroborate-catalyzed cycloisomerization of ynamides

A silver catalyzed-cycloisomerization of N-Boc protected ynamides has been developed under mild reaction conditions to provide a wide range of oxazol-2(3H)-ones in good to excellent yields. Moreover, the acid-promoted Pictet-Spengler cyclization of oxazol

Synthesis of functionalized oxazolones by a sequence of Cu(ll)- And Au(l)-catalyzed transformations

A study concerning a two-step sequence leading to the formation of diversely 1,5-disubstituted oxazolones is described. The mild conditions employed allow the efficient and rapid synthesis of a variety of such compounds via an initial Cu(II)-catalyzed coupling of a bromoalkyne with a secondary tert-butyloxycarbamate followed by a Au(l)-catalyzed cycloisomerization of the N-alkynyl tert-butyloxycarbamates thus obtained.