30069-65-9

Basic information

• Product Name: 3-phenylnaphthalen-1-ol
• Synonyms: 3-phenylnaphthalen-1-ol;3-phenylnaphthlaene-1-ol
• CAS NO: 30069-65-9
• Molecular Formula: C₁₆H₁₂O
• Molecular Weight: 220.26588
• EINECS: -0
• Mol File: 30069-65-9.mol
• Article Data: 28

Chemical Properties

• Melting Point: 96-97.5 °C(Solv: chloroform (67-66-3); hexane (110-54-3))
• Boiling Point: 417.4±24.0 °C(Predicted)
• Appearance: /
• Density: 1.176±0.06 g/cm3(Predicted)
• PKA: 9.28±0.40(Predicted)
• CAS DataBase Reference: 3-phenylnaphthalen-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenylnaphthalen-1-ol(30069-65-9)
• EPA Substance Registry System: 3-phenylnaphthalen-1-ol(30069-65-9)

Safety Data

• Hazardous Substances Data: 30069-65-9(Hazardous Substances Data)

Usage

General Description

3-phenylnaphthalen-1-ol is a chemical compound that belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond. It is notable for its unique structure, which involves a naphthalene component (a polycyclic aromatic hydrocarbon composed of two fused benzene rings) and a phenyl group (a functional group directly attached to a naphthalene component). The 'ol' suffix indicates the presence of an alcohol group in its molecular structure. 3-phenylnaphthalen-1-ol has a high boiling point and is soluble in alcohol. Its practical applications vary, and it's often used for research purposes.

Upstream product

• 30069-66-0 phenyl-acetic acid-(3-phenyl-[1]naphthyl ester) 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 93-91-4 1-phenylbutan-1,3-dione 
• 2142-70-3 2-iodoacetophenone 
• 98-86-2 acetophenone 
• 604-44-4 4-chloronaphthalen-1-ol 
• 108-86-1 bromobenzene 
• 106914-36-7 (E)-N,N-diethyl-3-phenylbut-2-enamide 
• 20718-17-6 2-(dimethyl(oxo)-λ⁶-sulfaneylidene)-1-phenylethan-1-one 
• 6048-29-9 triphenylphenacylphosphonium bromide 
• 551-93-9 2-aminoacetophenone 
• 53067-92-8 2-(2-acetylphenyl)-1-phenylethan-1-one 
• 97-72-3 2-Methylpropionic anhydride 
• 536-74-3 phenylacetylene 

Downstream Products

• 612-94-2 2-phenylnaphthalene 
• 30069-66-0 phenyl-acetic acid-(3-phenyl-[1]naphthyl ester) 
• 850650-61-2 3-phenylnaphthalene-1-yl trifluoromethanesulfonate 
• 1262778-24-4 3,8-diphenylnaphthalen-1-yl acetate 
• 587833-37-2 3,3'-diphenyl-<2,2'-binaphthalene>-1,1'-diol 
• 175223-61-7 (+/-)-vanol hydrogen phosphate 

Relevant articles and documents

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.

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

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