17762-72-0

Basic information

• Product Name: 2-phenyl-1,3-oxazinane
• Synonyms: (2H)1,3-Oxazine, tetrahydro-2-phenyl-; 2H-1,3-Oxazine, tetrahydro-2-phenyl-
• CAS NO: 17762-72-0
• Molecular Formula: C₁₀H₁₃NO
• Molecular Weight: 163.2163
• Mol File: 17762-72-0.mol

Chemical Properties

• Boiling Point: 273.1°C at 760 mmHg
• Flash Point: 105.3°C
• Density: 1.034g/cm³
• Vapor Pressure: 0.00584mmHg at 25°C
• Refractive Index: 1.518
• CAS DataBase Reference: 2-phenyl-1,3-oxazinane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-1,3-oxazinane(17762-72-0)
• EPA Substance Registry System: 2-phenyl-1,3-oxazinane(17762-72-0)

Safety Data

• Hazardous Substances Data: 17762-72-0(Hazardous Substances Data)

Upstream product

• 5433-11-4 N-Benzyliden-3-hydroxy-1-propanamin 
• 100-52-7 benzaldehyde 
• 156-87-6 propan-1-ol-3-amine 

Downstream Products

• 1161789-85-0 5-ethoxycarbonyl-6-(toluene-4-sulfinylmethyl)-4-phenyl-3,4-dihydropyrimidin-2(1H)-one 
• 883-93-2 2-Phenylbenzothiazole 
• 833-50-1 2-phenylbenzo[d]oxazole 
• 739-88-8 1-benzyl-2-phenyl-1H-1,3-benzimidazole 
• 716-79-0 2-phenyl-1H-benzoimidazole 
• 121998-76-3 2-phenyl-2,3-dihydro-4(1H)-quinazolinone 
• 5464-92-6 1-phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 3240-95-7 N-benzylidene-2-phenylethanamine 
• 63768-20-7 (rac)-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 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 
• 33761-65-8 1-phenyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline hydrochloride 
• 53219-37-7 diethyl 1,4-dihydro-2,6-dimethyl-1,4-diphenyl-3,5-pyridinedicarboxylate 
• 16979-93-4 N-benzylidene-2-(1H-indol-3-yl)ethylamine 

Relevant articles and documents

Efficient oxidative synthesis of 2-oxazolines

New methodology for the synthesis of variously substituted 2-oxazolines and one dihydrooxazine using aldehydes, amino alcohols, and N-bromosuccinimide as an oxidizing agent is described. This one-pot synthesis is characterized by mild reaction conditions, broad scope, high yields, and its preparative simplicity. Georg Thieme Verlag Stuttgart.

Ring-Chain Tautomerism in 1,3-Oxazines

A comparative study on the ring-chain tautomerism of 49 2-(substituted-phenyl) tetrahydro-1,3-oxazines of seven different types, namely, tetrahydro-1,3-oxazines 3,r-8a,c-2,c-4a- and r-8a,c-2,t-4a-1,3-perhydrobenzoxazines 5 and 7,r-8a,c-2,c-4- and r-8a,c-2,t-4a-1,3-perhydrobenzoxazines 9 and 11, 3,4-dihydro-2H-1,3-benzoxazines 12, and 1,2-dihydro-4H-3,1-benzoxazines 13, pointed out that in all cases the equilibria can be described with a simple equation, log Kx = (0.76 +/- 0.04)?+ + logKX=H where Kx = /(X/H).A factor c illustrating the sum of ster ic and electronic effects of substituents at C-4,C-5, and C-6 has also been introduced