36159-76-9

Basic information

• Product Name: 1-Hydroxy-4-phenylnaphthaline
• Synonyms: 1-Hydroxy-4-phenylnaphthalene;1-Hydroxy-4-phenylnaphthaline;4-Phenyl-1-naphthalenol;4-Phenyl-1-naphthol;4-phenylnaphthalen-1-ol（WS202208）
• CAS NO: 36159-76-9
• Molecular Formula: C₁₆H₁₂O
• Molecular Weight: 220.26588
• Mol File: 36159-76-9.mol
• Article Data: 15

Chemical Properties

• Melting Point: 140℃
• Boiling Point: 379℃
• Flash Point: 182℃
• Appearance: /
• Density: 1.176
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-Hydroxy-4-phenylnaphthaline(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hydroxy-4-phenylnaphthaline(36159-76-9)
• EPA Substance Registry System: 1-Hydroxy-4-phenylnaphthaline(36159-76-9)

Safety Data

• Hazardous Substances Data: 36159-76-9(Hazardous Substances Data)

Usage

General Description

1-Hydroxy-4-phenylnaphthaline, also known as 4-Hydroxy-1-phenylnaphthalene, is a chemical compound that belongs to the family of naphthalene derivatives. It is a yellow solid with a molecular formula C17H12O, and it is primarily used as a fluorescent dye and optical brightener in a variety of applications, including in the textile industry to enhance the whiteness and brightness of fabrics. It is also used in the manufacturing of fluorescent and optical brightening agents, as well as in research and development for chemical synthesis. 1-Hydroxy-4-phenylnaphthaline is known to have low toxicity and is generally considered to be safe for use in these applications.

Upstream product

• 14576-47-7 2-bromo-4-phenyl-3,4-dihydro-2H-naphthalen-1-one 
• 72774-00-6 1-methoxy-4-phenylnaphthalene 
• 78250-27-8 1-phenyl-4-hydroxy-2-naphthoic acid 
• 87833-80-5 1-amino-4-phenylnaphthalene 
• 111385-41-2 1-hydroxy-4-phenyl-2-naphthoic acid 
• 7498-88-6 4,4-diphenylbut-3-enoic acid 
• 127-09-3 sodium acetate 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 91-66-7 N,N-diethylaniline 
• 7746-94-3 5,5-diphenyldihydrofuran-2(3H)-one 
• 78250-37-0 1-Acetoxy-4-phenylnaphthalene 
• 604-44-4 4-chloronaphthalen-1-ol 

Downstream Products

• 73671-07-5 4-phenylnaphthalene-1,2-dione 
• 108639-42-5 Diphenyl-carbamic acid 4-phenyl-naphthalen-1-yl ester 
• 108639-37-8 4-phenyl-1-naphthyl 2'-oxocyclohexyl ether 
• 107801-16-1 Bis-<4-phenyl-naphthalin-(2)>-indigoid 
• 72774-00-6 1-methoxy-4-phenylnaphthalene 
• 78250-39-2 Dimethyl-[2-(4-phenyl-naphthalen-1-yloxy)-ethyl]-amine 
• 78250-38-1 (Benzyl)<β-(4-phenyl-1-naphthyloxy)ethyl>dimethylammonium bromide 
• 108660-60-2 5-phenylnaphtho<1,2-b>benzofuran 
• 113057-92-4 5-phenylbenzo[a]phenazine 

Relevant articles and documents

2,2,4,6-Tetraaryl-2H-benzo[h]chromenes: The influence of electronic communication between aryl substituents on their photochromism

A series of photochromic 2,2,4,6-tetraaryl-2H-benzo[h]chromenes have been efficiently synthesised by two complementary strategies employing the condensation of 1,1,3-triarylprop-2-yn-1-ols with 4-substituted 1-naphthols and Suzuki cross-coupling chemistry

Rapid, Operationally Simple, and Metal-free NBS Mediated One-pot Synthesis of 1,2-Naphthoquinone from 2-Naphthol

A metal-free, one-pot synthesis of 1,2-naphthoquinone was accomplished from 2-naphthol by utilizing economically cheap NBS under open air conditions. Initial formation of 1,1-dibromonaphthalen-2-one and subsequent transformation afforded the 1,2-naphthoquinone. This oxidation was completed within 30 min and had broad substrate scope. Moreover, this system tolerated heterocyclic systems and was also applicable to 1,3-dicarbonyl systems. This practical approach with short reaction times, a simple workup, and insensitivity to moisture could override the usage of expensive and hazardous oxidizing and metal reagents. (Figure presented.).

ORGANOMETALLIC COMPLEX FOR ORGANIC LIGHT-EMITTING LAYER AND ORGANIC LIGHT-EMITTING DIODE USING THE SAME

An organometallic complex represented by Formula 1 is provided. An organic light-emitting diode using the organometallic complex exhibits improved current and power efficiency and long lifetime.