90917-82-1

Basic information

• Product Name: 5-methyl-4-phenyl-4,5-dihydro-oxazol-2-ylamine
• Synonyms: 5-methyl-4-phenyl-4,5-dihydro-oxazol-2-ylamine
• CAS NO: 90917-82-1
• Molecular Weight: 176.218
• Mol File: 90917-82-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-methyl-4-phenyl-4,5-dihydro-oxazol-2-ylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methyl-4-phenyl-4,5-dihydro-oxazol-2-ylamine(90917-82-1)
• EPA Substance Registry System: 5-methyl-4-phenyl-4,5-dihydro-oxazol-2-ylamine(90917-82-1)

Safety Data

• Hazardous Substances Data: 90917-82-1(Hazardous Substances Data)

Upstream product

• 873-66-5 1-propenylbenzene 
• 3315-16-0 silver cyanate 
• 57-13-6 urea 
• 52500-61-5 2-hydroxy-1-phenylpropylamine 
• 103-79-7 1-phenyl-acetone 
• 25355-34-4 1-phenyl-propane-1,2-dione 1-oxime 
• 506-68-3 bromocyane 
• 1196-45-8 (1-bromoethyl)benzyl bromide 

Downstream Products

• 19901-87-2 (1R,2S/1R,2R)-1-amino-1-phenylpropan-2-ol 
• 19901-87-2 threo-amino-1-phenyl-1-propanol-2 

Relevant articles and documents

Regioselective Formal [3+2] Cycloadditions of Urea Substrates with Activated and Unactivated Olefins for Intermolecular Olefin Aminooxygenation

A new class of intermolecular olefin aminooxygenation reaction is described. This reaction utilizes the classic halonium intermediate as a regio- and stereochemical template to accomplish the selective oxyamination of both activated and unactivated alkenes. Notably, urea chemical feedstock can be directly introduced as the N and O source and a simple iodide salt can be utilized as the catalyst. This formal [3+2] cycloaddition process provides a highly modular entry to a range of useful heterocyclic products with excellent selectivity and functional-group tolerance.

2,3,6,7-Tetrahydro-2-thioxo-4H-oxazolo[3,2-a]-1,3,5 triazin-4-ones

A compound of the formula STR1 wherein R1 is phenyl or substituted phenyl when R2 is hydrogen or lower alkyl; and R2 is phenyl or substituted phenyl when R1 is hydrogen or lower alkyl. These compounds are useful as anti-inflammatory agents.