85-15-4

Basic information

• Product Name: 2-Methylnaphth[1,2-d]oxazole
• Synonyms: 2-d]oxazole,2-methyl-naphth[;2-d]oxazole,2-methyl-Naphth[1;Naphth[1,2-d]oxazole, 2-methyl-;2-METHYLNAPHTHO[1,2D]OXAZOLE;2-METHYLNAPHTH[1,2-D]OXAZOLE;2-METHYLNAPHTHYL[1,2-D]OXAZOLE;2-Methylnaphtho[1,2d]oxazole 98%;2-Methylbenzo[e][1,3]benzoxazole
• CAS NO: 85-15-4
• Molecular Formula: C₁₂H₉NO
• Molecular Weight: 183.21
• EINECS: 201-589-9
• Mol File: 85-15-4.mol
• Article Data: 6

Chemical Properties

• Melting Point: -15°C
• Boiling Point: 300 °C
• Flash Point: 131.1 °C
• Appearance: light yellow oil liquid
• Density: 1.182
• Vapor Pressure: 0.000565mmHg at 25°C
• Refractive Index: 1.6350 to 1.6390
• PKA: 2.16±0.30(Predicted)
• CAS DataBase Reference: 2-Methylnaphth[1,2-d]oxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methylnaphth[1,2-d]oxazole(85-15-4)
• EPA Substance Registry System: 2-Methylnaphth[1,2-d]oxazole(85-15-4)

Safety Data

• Hazardous Substances Data: 85-15-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H9NO/c1-8-13-12-10-5-3-2-4-9(10)6-7-11(12)14-8/h2-7H,1H3

Upstream product

• 127-09-3 sodium acetate 
• 135-19-3 β-naphthol 
• 50629-48-6 2-trimethylsilyloxy-3,4-dihydronaphthalene 
• 108-24-7 acetic anhydride 
• 2834-92-6 1-amino-2-naphthol 
• 117-93-1 1-acetylamino-naphthalen-2-ol 
• 2636-79-5 1,2-naphthoquinone 1-oxime 
• 75-03-6 ethyl iodide 

Downstream Products

• 117-93-1 1-acetylamino-naphthalen-2-ol 
• 5095-88-5 2-(4-chloro-styryl)-naphtho[1,2-d]oxazole 

Relevant articles and documents

Metallic Compound and Organic Electroluminescence Device Comprising the Same

The present invention relates to a light-emitting transition metal compound represented by the Chemical Formula 1 and Chemical Formula 2 and an organic electroluminescence device including the same. In the Chemical Formulae 1 and 2, M is Ir, Pt, Rh, Re, Os, and the like, m is 2 or 3, n is 0 or 1, the sum of m and n is 3, provided that the sum of m and n is 2 when M is Pt, X, and Z are the same or different, N or P, and Y and Q are O, S, or Se, R1 and R5 are hydrogen, a C1 to C20 alkyl excluding an aromatic cyclic substituent, a cycloalkyl, a halogen, a linear or branched substituent including at least one halogen, or a linear or branched substituent including at least one heteroatom, and R2, R3, R4, R6, R7, R8, R9, and R10 are hydrogen, a C1 to C20 alkyl, an aryl, a cycloalkyl, a halogen, a linear or branched substituent including at least one halogen, a linear or branched substituent including at least one heteroatom, carbonyl, vinyl, or acetylenyl, or may form a cycle, and may be the same or different.

METALLIC COMPOUND AND ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THE SAME

The present invention relates to a light-emitting transition metal compound represented by the Chemical Formula 1 and Chemical Formula 2 and an organic electroluminescence device including the same. In the Chemical Formulae 1 and 2, M is Ir, Pt, Rh, Re, Os, and the like, m is 2 or 3, n is 0 or 1 , the sum of m and n is 3, provided that the sum of m and n is 2 when M is Pt, X, and Z are the same or different, N or P, and Y and Q are O, S, or Se, R1 and R5 are hydrogen, a C1 to C20 alkyl excluding an aromatic cyclic substituent, a cycloalkyl, a halogen, a linear or branched substituent including at least one halogen, or a linear or branched substituent including at least one heteroatom, and R2, R3, R4, R6, R7, R8, R9, and R10 are hydrogen, a C1 to C20 alkyl, an aryl, a cycloalkyl, a halogen, a linear or branched substituent including at least one halogen, a linear or branched substituent including at least one heteroatom, carbonyl, vinyl, or acetylenyl, or may form a cycle, and may be the same or different.

Reaction of silyl enol ethers with xenon difluoride in MeCN: Evidence for a nonclassical radical cation intermediate

(matrix presented). The reactions of xenon difluoride in MeCN solution in Pyrex flasks with a series of TMS enol ethers have been investigated. The types of products formed are dependent on the structures of individual enol ethers, but under these conditions all products are consistent with a mechanism involving single electron transfer to un-ionized XeF2 giving a radical cation and subsequent formation of an α-fluoroketone, together with some ketone formation. The results suggest that if the radical cation is particularly stable, fluorodesilylation leads to radical formation, and solvent-derived products are then observed. Using other solvents, such as CFCl3 and C6F6, much more complex mixtures of products are obtained, and this is attributed to a different mode of reaction of xenon difluoride involving ionization to FXe+.