13727-29-2

Basic information

• Product Name: 1-phenyl-5,6-dihydro-4H-1,3-oxazine
• Synonyms: 1-phenyl-5,6-dihydro-4H-1,3-oxazine
• CAS NO: 13727-29-2
• Molecular Weight: 215.295
• Mol File: 13727-29-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-phenyl-5,6-dihydro-4H-1,3-oxazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-5,6-dihydro-4H-1,3-oxazine(13727-29-2)
• EPA Substance Registry System: 1-phenyl-5,6-dihydro-4H-1,3-oxazine(13727-29-2)

Safety Data

• Hazardous Substances Data: 13727-29-2(Hazardous Substances Data)

Upstream product

• 6282-02-6 N-(hydroxymethyl)benzamide 
• 110-83-8 cyclohexene 
• 55-21-0 benzamide 
• 156025-77-3 N-(triflyloxy)-N-methylbenzamide 
• 98-88-4 benzoyl chloride 
• 2446-50-6 N-hydroxy-N-methylbenzamide 
• 137570-69-5 N-(isopropoxymethyl)benzamide 
• 50-00-0 formaldehyd 

Downstream Products

• 20617-32-7 cis-2-benzoylaminomethyl-1-cyclohexanol 
• 94819-68-8 trans-5,6-tetramethylene-5,6-dihydro-2-phenyl-<4H>-1,3-thiazine 
• 77612-17-0 N-Benzyl-cis-2-aminomethylcyclohexanol 
• 77612-17-0 cis-N-benzyl-2-aminomethyl-1-cyclohexanol 
• 126675-35-2 cis-2-(N-cyclohexylaminomethyl)-1-cyclohexanol hydrochloride 
• 79658-23-4 cis-2-(N-isopropylaminomethyl)-1-cyclohexanol hydrochloride 
• 151095-68-0 N-Benzoyl-2-hydroxy-hexahydrobenzylamin 

Relevant articles and documents

Synthesis of alicyclic N-substituted 1,3-amino alcohols via 1,3-oxazines

(Chemical Equation Presented) Alicyclic N-substituted 1,3-amino alcohols 13-18 were prepared in a facile way in a one-pot procedure from 1,3-oxazines 5-8 in the presence of a ketone 9-12. The complex reaction involves palladium-catalyzed reduction, debenz

A Facile Preparation of N-(Isopropoxyalkyl) Amides by Generation and Trapping of N-Acyliminium Ions from Ionization-Rearrangement Reactions of N-Triflyloxy Amides

A series of hydroxamic acids were converted to N-triflyloxy amides which were heated in 2-propanol to give N-(1-isopropoxyalkyl) amides in high yields.The method is simple, direct, and extremely tolerant of structural diversity both in the N-acyl group, a

STEREOCHEMICAL STUDIES, 80. CYCLIC AMINOALCOHOLS AND RELATED COMPOUNDS, 26. PREPARATION OF CIS-2-(ALKYLAMINOMETHYL)- AND (ARALKYLAMINOMETHYL)-1-CYCLANOLS FROM OLEFINS VIA THE 5,6-DIHYDRO-4H-1,3-OXAZINE DERIVATIVES

Cycloalkenes were allowed to react with N-(hydroxymethyl)alkyl- or -arylamides in the presence of concentrated sulfuric acid in glacial acetic acid, using the method suggested by Schmidt.In the majority of cases, the reaction yielded the corresponding cis