30069-65-9

Usage

Uses

Used in Research Applications:
3-phenylnaphthalen-1-ol is used as a research compound for its unique structure and properties. It is often utilized in the study of organic chemistry and the synthesis of various chemical compounds.
Used in Chemical Synthesis:
3-phenylnaphthalen-1-ol is used as a starting material or intermediate in the synthesis of more complex organic compounds, particularly those with potential applications in pharmaceuticals, materials science, or other specialized fields.
Used in Pharmaceutical Development:
3-phenylnaphthalen-1-ol is used as a potential candidate for the development of new pharmaceuticals, given its unique structure and the presence of an alcohol group, which may allow for further functionalization and the creation of new drug molecules.
Used in Material Science:
3-phenylnaphthalen-1-ol is used as a component in the development of new materials, such as polymers or other advanced materials, where its unique structure and properties may contribute to desired characteristics, such as improved stability or enhanced performance.

Upstream product

• 132-86-5 1,3-dihydroxynaphthalene 
• 71-43-2 benzene 
• 30069-66-0 phenyl-acetic acid-(3-phenyl-[1]naphthyl ester) 
• 97-72-3 2-Methylpropionic anhydride 
• 536-74-3 phenylacetylene 
• 103-80-0 phenylacetyl chloride 
• 53067-92-8 2-(2-acetylphenyl)-1-phenylethan-1-one 
• 2142-70-3 2-iodoacetophenone 
• 98-86-2 acetophenone 
• 551-93-9 2-aminoacetophenone 
• 90767-17-2 3-bromo-1-hydroxynaphthalene 
• 98-80-6 phenylboronic acid 
• 4411-98-7 3,4-diphenyl-crotonic acid 
• 604-44-4 4-chloronaphthalen-1-ol 

Downstream Products

• 2348-77-8 2-phenyl[1,4]naphthoquinone 
• 51670-51-0 3-phenylnaphthalene-1,2-dione 
• 612-94-2 2-phenylnaphthalene 
• 30069-66-0 phenyl-acetic acid-(3-phenyl-[1]naphthyl ester) 
• 587833-37-2 3,3'-diphenyl-<2,2'-binaphthalene>-1,1'-diol 
• 850650-61-2 3-phenylnaphthalene-1-yl trifluoromethanesulfonate 
• 175223-61-7 (+/-)-vanol hydrogen phosphate 
• 51670-50-9 <3-Phenyl-naphthyl-(1)-oxy>-essigsaeure 

Relevant academic research and scientific papers

Enantiodivergent Kinetic Resolution of 1,1′-Biaryl-2,2′-Diols and Amino Alcohols by Dipeptide-Phosphonium Salt Catalysis Inspired by the Atherton–Todd Reaction

A highly enantiodivergent organocatalytic method is disclosed for the synthesis of atropisomeric biaryls via kinetic resolution inspired by a dipeptide-phosphonium salt-catalyzed Atherton–Todd (A-T) reaction. This flexible approach led to both R- and S-enantiomers by fine-tuning of bifunctional phosphonium with excellent selectivity factors (s) of up to 1057 and 525, respectively. The potential of newly synthesized O-phosphorylated biaryl diols was illustrated by the synthesis of axially chiral organophosphorus compounds. Mechanistic investigations suggest that the bifunctional phosphonium halide catalyst differentiates between the in-situ-generated P-species in the A-T process, mainly involving phosphoryl chloride and phosphoric anhydride, thus leading to highly enantiodivergent O-phosphorylation reactions. Furthermore hydrogen bonding interactions between the catalysts and phosphorus molecules were crucial in asymmetric induction.

Ruthenium-catalyzed coupling of α-carbonyl phosphoniums with sulfoxonium ylidesviaC-H activation/Wittig reaction sequences

A Ru(ii)-catalyzed coupling of various α-carbonyl phosphoniums with sulfoxonium ylides has been realized for the facile synthesis of 1-naphthols in good to excellent yields. This oxidant-free transformation proceeds through Ru-catalyzed C-H activation of phosphoniums, Ru-carbene insertion, and intramolecular Wittig reaction processes.

Cu(II)-Catalyzed 6π-Photocyclization of Non-6πSubstrates

This research successfully achieved a Cu(II)-catalyzed 6π-photocyclization of non-6πsubstrates. The photoenolization converts ortho-alkylphenyl alkynl ketones into a triene-type intermediate which undergoes the subsequent 6π-photocyclization to give napht

Chemo- and Regioselective Catalyst-Controlled Carbocyclization of Alkynyl Ketones: Rapid Synthesis of 1-Indanones and 1-Naphthols

A catalyst-controlled intramolecular carbocyclization of 2-alkynyl aryl ketones is presented. Under rhodium(III) catalysis, 1-indanones are formed through 5-exo-dig carbocyclizations with exclusive chemo-, regio- and stereoselectivity. When catalyzed by copper(I), 1-naphthols are obtained through 6-endo-dig carbocyclizations with exclusive chemo- and regioselectivity.

AMINE-SUBSTITUTED NAPHTHALENE DERIVATIVES AND ORGANIC LIGHT EMITTING DIODES INCLUDING THE SAME

Disclosed are amine-substituted naphthalene derivatives and organic light emitting diodes including the same. In the organic light emitting diodes, at least one of the amine-substituted naphthalene derivatives is employed in a hole auxiliary layer interpo

Anthracene derivatives and organic light emitting devices comprising the same

An anthracene derivative represented by Formula 1 is disclosed. An organic light-emitting device including an anode, a cathode, and an organic layer between the anode and the cathode, where the organic layer includes at least one anthracene derivative represented by Formula 1, is also disclosed. A method of manufacturing the organic light-emitting device is also disclosed.

Reaction of arynes with trifluoroacetylated β-diketones: Novel formation of isocoumarins and phenanthrenes

Polysubstituted isocoumarins were synthesized by the reaction of substituted 2-(trimethylsilyl)aryl triflates with trifluoromethylated β-diketones in the presence of CsF. The reaction proceeded through carbon-carbon bond insertion of aryne and intramolecular cyclization to form intermediates of alcohol anions, which extruded trifluoromethyl anion to afford isocoumarins. By using CuBr as a catalyst, 2 eq. of aryne reacted with β-diketones to afford phenanthrenes and 1,2-diarylethanones. Although reaction of 2-(trimethylsilyl)phenyl triflate with 1,1,1-trifluoro-4′-methylbenzoylacetone in the presence of CsF gave 3-(4′-methylphenyl)isocoumarin in 67% yield, addition of 0.2 eq. of CuCN resulted in the formation of 9-(4-methylbenzoyl)-10-trifluoromethylphenanthrene in 35% yield.

aromatic compound having fused cyclic substituent in aromatic ring and organic light-emitting diode including the same

The present invention relates to a compound having a cyclic substituent fused with a cyclic ring and an organic light emitting diode including the same, and more particularly, to a compound for an organic light emitting diode represented by chemical formula A and an organic light emitting diode including the same. In chemical formula A, X is a substituent having structural formula X, Y is a substituent of structural formula Y1, n is an integer from 1 to 4, and structural formulas X and Y1 are the same as described in detailed description of the present invention.

ORGANIC LIGHT-EMITTING DIODE WITH HIGH EFFICIENCY AND LONG LIFETIME

Disclosed herein is an organic light-emitting diode, comprising: an organic light-emitting diode, comprising: a first electrode; a second electrode facing the first electrode; a light-emitting layer intercalated between the first electrode and the second electrode, wherein the light-emitting layer comprises at least one of the amine compounds represented by Chemical Formula A or B, and at least one of the anthracene compounds represented by Chemical Formula C.

An electroluminescent compound and an electroluminescent device comprising the same

The present invention relates to an organic light emitting compound applied to an organic electroluminescent device. The organic light emitting compound is represented by [chemical formula 1] and has a substituent represented by [structural formula 1] or [structural formula 2]. When the organic light emitting compound is applied as a host compound or a dopant compound in a light emitting layer, the organic electroluminescent device with excellent light emitting properties such as driving voltage, brightness, and durability can be provided. [chemical formula 1] [structural formula 1] [structural formula 2]COPYRIGHT KIPO 2016