20515-61-1

Basic information

• Product Name: Oxazolidine, 4,4-dimethyl-2-phenyl-
• Synonyms: 4,4-Dimethyl-2-phenyl-oxazolidin;1,3-Oxazolidine,4,4-dimethyl-2-phenyl;4,4-dimethyl-2-phenyloxazolidine;2-Phenyl-4,4-dimethyl-oxazolidin;2-phenyl-4,4-dimethyl oxazolidine;Oxazolidine,4,4-dimethyl-2-phenyl
• CAS NO: 20515-61-1
• Molecular Formula: C11H15NO
• Molecular Weight: 177.246
• Mol File: 20515-61-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Oxazolidine, 4,4-dimethyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazolidine, 4,4-dimethyl-2-phenyl-(20515-61-1)
• EPA Substance Registry System: Oxazolidine, 4,4-dimethyl-2-phenyl-(20515-61-1)

Safety Data

• Hazardous Substances Data: 20515-61-1(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 71-43-2 benzene 
• 22563-90-2 2-Benzalamino-isobutanol 
• 124-68-5 2-Amino-2-methyl-1-propanol 

Downstream Products

• 51200-90-9 3-benzyl-4,4-dimethyl-oxazolidine 
• 60980-23-6 2-phenyl-3-chloroacetyl-4,4-dimethyl oxazolidine 
• 19312-06-2 4,5-dihydro-4,4-dimethyl-2-phenoxazole 
• 739-88-8 1-benzyl-2-phenyl-1H-1,3-benzimidazole 
• 121998-76-3 2-phenyl-2,3-dihydro-4(1H)-quinazolinone 
• 10133-74-1 N-benzylidene-2-(3',4'-dimethoxyphenyl)ethylamine 
• 4118-36-9 6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline 
• 16979-93-4 (E)-N-(2-(1H-indol-3-yl)ethyl)-1-phenylmethanimine 
• 22563-90-2 2-Benzalamino-isobutanol 
• 3240-95-7 N-benzylidene-2-phenylethanamine 
• 10133-74-1 N-phenylmethylene-2-(3,4-dimethoxyphenyl)ethylamine 
• 1165-06-6 Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 3790-45-2 1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline 
• 53219-37-7 diethyl 1,4-dihydro-2,6-dimethyl-1,4-diphenyl-3,5-pyridinedicarboxylate 

Relevant articles and documents

Synthesis of dioxolanes and oxazolidines by silica gel catalysis

Abstract: Ethylene glycol condensed with carbonyl compounds in the presence of silica gel or alumina, without solvent and under pressure, affords 1,3-dioxolanes. 2-Amino-2-methylpropanol also condensed with carbonyl compounds in the presence of silica gel or an acid-activated clay, without solvent and under pressure, produces oxazolidines. To explain these results, we propose that the glycol and the aminopropanol react with Br?nsted (H+) and Lewis acid sites (Si and Al) located on the surface of the catalysts, leading to the products via various ionic intermediates.

HYDROXY SCHIFF BASE-OXAZOLIDINE TAUTOMERISM: APPARENT BREAKDOWN OF BALDWIN'S RULES

The tautomerism between hydroxy Schiff bases, X=C6H4CR=NCMe2CH2OH (R=H, Me, C6H5; X is a range of substituents) and X=C6H4CR=NC6H4(o-CH2OH), and the corresponding ring closed systems, oxazolidines and dihydrobenzoxazines, has been investigated.In all case