3574-02-5

Basic information

• Product Name: 2-phenylnaphtho[1,2-d][1,3]oxazole
• Synonyms: 2-phenylnaphtho[1,2-d][1,3]oxazole
• CAS NO: 3574-02-5
• Molecular Formula: C₁₇H₁₁NO
• Molecular Weight: 245.27534
• Mol File: 3574-02-5.mol
• Article Data: 20

Chemical Properties

• Melting Point: 130-131 °C(Solv: water (7732-18-5); methanol (67-56-1))
• Boiling Point: 397°C at 760 mmHg
• Flash Point: 167°C
• Appearance: /
• Density: 1.232g/cm³
• Vapor Pressure: 3.75E-06mmHg at 25°C
• Refractive Index: 1.7
• PKA: 0.82±0.30(Predicted)
• CAS DataBase Reference: 2-phenylnaphtho[1,2-d][1,3]oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenylnaphtho[1,2-d][1,3]oxazole(3574-02-5)
• EPA Substance Registry System: 2-phenylnaphtho[1,2-d][1,3]oxazole(3574-02-5)

Safety Data

• Hazardous Substances Data: 3574-02-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H11NO/c1-2-7-13(8-3-1)17-18-16-14-9-5-4-6-12(14)10-11-15(16)19-17/h1-11H

Upstream product

• 72771-51-8 1-benzamido-2-naphthol 
• 40447-11-8 3-benzoyl-1-cyclohexyl-2-phenylaziridine 
• 131-91-9 1-Nitroso-2-naphthol 
• 1198-27-2 1-aminonaphthalene-2-ol hydrochloride 
• 100-52-7 benzaldehyde 
• 2834-92-6 1-amino-2-naphthol 
• 2211-61-2 trans-1-cyclohexyl-2-phenyl-3-benzoylaziridine 
• 4476-14-6 1,2-naphthoquinone-1-benzimide 
• 7629-77-8 2-phenyl-3H-naphtho[2,1-b][1,4]oxazin-3-one 
• 69321-38-6 1-nitroso-2-naphthol 
• 100-39-0 benzyl bromide 
• 15206-55-0 methyl 2-oxo-2-phenylacetate 
• 634-42-4 N-1-naphthalenyl-benzamide 
• 233-70-5 naphtho[1,2-d]oxazole 

Downstream Products

• 2834-92-6 1-amino-2-naphthol 
• 65-85-0 benzoic acid 

Relevant articles and documents

Chemodivergent Synthesis of Oxazoles and Oxime Ethers Initiated by Selective C-N/C-O Formation of Oximes and Diazo Esters

Chemodivergent reactions of oximes and diazo esters involving Rh-catalyzed [3+2] annulation and photodriven O-H insertion have been developed to generate oxazoles and oxime ethers. A range of aldehyde and ketone oximes reacted with α-diazocarbonyl compounds in a controllable manner in which functional groups, including ketone, ester, amide, ether, thiol ether, silane, alkene, allene, and alkyne groups, were well tolerated.

Radical cascade synthesis of azoles: via tandem hydrogen atom transfer

A radical cascade strategy for the modular synthesis of five-membered heteroarenes (e.g. oxazoles, imidazoles) from feedstock reagents (e.g. alcohols, amines, nitriles) has been developed. This double C-H oxidation is enabled by in situ generated imidate

ORGANIC COMPOUNDS AND ORGANIC ELECTRO LUMINESCENCE DEVICE COMPRISING THE SAME

The present invention relates to a novel compound and an organic electroluminescent device comprising the same. A compound according to the present invention is used for an organic layer, preferably a light emitting layer, a hole transporting layer, an electron transport layer, or an electron transport auxiliary layer of the organic electroluminescent device, thereby being able to improve luminous efficiency, driving voltage, lifespan and the like of the organic electroluminescent device.COPYRIGHT KIPO 2019