3585-81-7

Basic information

• Product Name: Oxaziridine, 2-(1,1-dimethylethyl)-3-phenyl-, (2R,3R)-rel-
• CAS NO: 3585-81-7
• Molecular Formula: C11H15NO
• Molecular Weight: 177.246
• Mol File: 3585-81-7.mol
• Article Data: 34

Chemical Properties

• CAS DataBase Reference: Oxaziridine, 2-(1,1-dimethylethyl)-3-phenyl-, (2R,3R)-rel-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxaziridine, 2-(1,1-dimethylethyl)-3-phenyl-, (2R,3R)-rel-(3585-81-7)
• EPA Substance Registry System: Oxaziridine, 2-(1,1-dimethylethyl)-3-phenyl-, (2R,3R)-rel-(3585-81-7)

Safety Data

• Hazardous Substances Data: 3585-81-7(Hazardous Substances Data)

Upstream product

• 6852-58-0 N-benzylidene tert-butylamine 
• 27151-60-6 1-t-butyl-3-phenylaziridin-2-one 
• 3376-24-7 (Z)-N-benzylidene-2-methylpropan-2-amine oxide 
• 3376-24-7 N-tert-butyl-α-phenylnitrone 
• 6852-58-0 (E)-N-benzylidene-2-methylpropan-2-amine 
• 100-52-7 benzaldehyde 
• 75-64-9 tert-butylamine 
• 497-19-8 sodium carbonate 
• 529-20-4 2-methylphenyl aldehyde 

Downstream Products

• 18150-81-7 N-(diphenylmethyl)-2-methylpropan-2-amine 
• 72995-56-3 4-benzyl-2-tert-butyl-3-phenyl-[1,2,4]oxadiazolidine-5-thione 
• 3376-24-7 N-tert-butyl-α-phenylnitrone 
• 5894-65-5 N-t-butylbenzamide 
• 6852-58-0 (E)-N-benzylidene-2-methylpropan-2-amine 
• 6852-58-0 N-benzylidene tert-butylamine 
• 100-52-7 benzaldehyde 
• 88015-31-0 N-butyl-2-(1-methylethyl)pyrrolidine 
• 88015-33-2 N-butyl-5-methyl-4-hexenamine 
• 106745-24-8 methyl N-tert-butyl-3-phenylisoxazolidine-5-carboxylate 
• 69849-46-3 N-tert-butyl-N-(1-phenylpentyl)amine 
• 54222-26-3 2-tert-butyl-4-(3-isocyanato-4-methyl-phenyl)-3-phenyl-[1,2,4]oxadiazolidin-5-one 
• 35105-50-1 (2-tert-butyl-3,4-diphenyl-[1,2,4]oxadiazolidin-5-ylidene)-phenyl-amine 
• 54222-28-5 2,2'-di-tert-butyl-3,3'-diphenyl-4,4'-(4-methyl-m-phenylene)-bis-[1,2,4]oxadiazolidin-5-one 

Relevant articles and documents

Weak base-promoted selective rearrangement of oxaziridines to amidesviavisible-light photoredox catalysis

The selective rearrangement of oxaziridines to amidesviaa single electron transfer (SET) pathway is unexplored. In this study, we present a weak base-promoted selective rearrangement of oxaziridines to amidesviavisible-light photoredox catalysis. The developed method shows excellent functional group tolerance with a broad substrate scope and good to excellent yields. Furthermore, control experiments and density functional theory (DFT) calculations are performed to gain insight into the reactivity and selectivity.

Atom economical synthesis of: N -alkylbenzamides via the iron(III) sulfate catalyzed rearrangement of 2-alkyl-3-aryloxaziridines in water and in the presence of a surfactant

A green and mild synthetic route to N-alkylbenzamides involves eco-friendly one pot synthesis of 2-alkyl-3-aryloxaziridines from N-alkylamines and benzaldehydes followed by iron(iii) sulfate catalyzed rearrangement to the corresponding amides in water as the solvent and in the presence of sodium dodecyl sulfate as the surfactant. This green approach affords N-alkylbenzamides in high overall yields under simple and minimum manipulation.

Hydrogen peroxide/dimethyl carbonate: A green system for epoxidation of: N -alkylimines and N -sulfonylimines. One-pot synthesis of N -alkyloxaziridines from N -alkylamines and (hetero)aromatic aldehydes

A green method for epoxidation of imines using an environmentally benign oxidant system, H2O2/dimethyl carbonate, was developed. N-Alkyloxaziridines were prepared in high yields from N-alkylamines and (hetero)aromatic aldehydes in one-pot fashion, whereas N-sulfonyloxaziridines have been prepared by using the same oxidant system and 5 mol% of Zn(OAc)2·2H2O as catalyst.