3140-01-0

Basic information

• Product Name: 2,4,6-Triphenylphenol
• Synonyms: 2,4,6-Triphenylphenol
• CAS NO: 3140-01-0
• Molecular Formula: C₂₄H₁₈O
• Molecular Weight: 322.39912
• Mol File: 3140-01-0.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 461.4°Cat760mmHg
• Flash Point: 216.7°C
• Appearance: /
• Density: 1.136g/cm³
• Vapor Pressure: 3.91E-09mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: 2,4,6-Triphenylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Triphenylphenol(3140-01-0)
• EPA Substance Registry System: 2,4,6-Triphenylphenol(3140-01-0)

Safety Data

• Hazardous Substances Data: 3140-01-0(Hazardous Substances Data)

Usage

General Description

2,4,6-Triphenylphenol is a chemical compound with the molecular formula C18H14O. It is a white crystalline solid and is commonly used as an antimicrobial and antifungal agent in a variety of consumer and industrial products including plastics, papers, and textiles. It is also utilized in the production of dyes, photographic chemicals, and pharmaceuticals. 2,4,6-Triphenylphenol is known for its ability to inhibit the growth of various microorganisms and has been studied for its potential use in controlling bacterial and fungal infections. However, there are concerns about its potential environmental and health impacts, and it is advised to use it with caution and according to safety guidelines.

InChI:InChI=1/C24H18O/c25-24-22(19-12-6-2-7-13-19)16-21(18-10-4-1-5-11-18)17-23(24)20-14-8-3-9-15-20/h1-17,25H

Upstream product

• 118-79-6 2,4,6-tribromophenol 
• 98-80-6 phenylboronic acid 
• 143-66-8 sodium tetraphenyl borate 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 5467-74-3 4-Bromophenylboronic acid 
• 108-95-2 phenol 
• 115292-92-7 2,4,6-triphenylanisole 
• 607-99-8 2,4,6-tribromoanisole 
• 13505-60-7 2-Acetoxy-2,4,6-triphenyl-cyclohexadien-(3,5)-on 
• 13505-55-0 4-Methoxy-2,4,6-triphenyl-cyclohexadien-(2,5)-on 
• 10384-15-3 2,4,6-triphenyl-4-(2,4,6-triphenyl-phenoxy)-cyclohexa-2,5-dienone 
• 75-52-5 nitromethane 
• 448-61-3 2,4,6-triphenylpyrylium tetrafluoroborate 
• 6864-20-6 2,4,6-triphenylaniline 

Downstream Products

• 10384-15-3 2,4,6-triphenyl-4-(2,4,6-triphenyl-phenoxy)-cyclohexa-2,5-dienone 
• 130096-31-0 Ta(OC₆H₂(C₆H₅)3)2Cl₃ 
• 4647-83-0 2,4,6-triphenylphenoxyl 
• 130096-35-4 Ta(OC₆H₂(C₆H₅)3)2(CH₂C₆H₄CH₃)3 
• 130096-39-8 Ta(OC₂₄H₁₇)(OC₂₄H₁₆)(C₈H₉)2 
• 13505-59-4 2-Methoxy-2,4,6-triphenyl-cyclohexadien-(3,5)-on 
• 65549-96-4 4,6-bis(4-tert-butylphenyl)-2-{4-tert-butyl-2-[2,4,6-tris(4-tert-butylphenyl)phenoxy]phenyl}phenol 
• 342607-37-8 C₇₂H₈₂O₂ 
• 19509-97-8 2,4,6-Triphenyl-o-chinolbenzoat 
• 4647-83-0 2,4,6-triphenylphenoxyl radical 
• 13505-60-7 2-Acetoxy-2,4,6-triphenyl-cyclohexadien-(3,5)-on 
• 13505-55-0 4-Methoxy-2,4,6-triphenyl-cyclohexadien-(2,5)-on 

Relevant articles and documents

A scalable and green one-minute synthesis of substituted phenols

A mild, green and highly efficient protocol was developed for the synthesis of substituted phenols via ipso-hydroxylation of arylboronic acids in ethanol. The method utilizes the combination of aqueous hydrogen peroxide as the oxidant and H2O2/HBr as the reagent under unprecedentedly simple and convenient conditions. A wide range of arylboronic acids were smoothly transformed into substituted phenols in very good to excellent yields without chromatographic purification. The reaction is scalable up to at least 5 grams at room temperature with one-minute reaction time and can be combined in a one-pot sequence with bromination and Pd-catalyzed cross-coupling to generate more diverse, highly substituted phenols.

Benzimidazole-based palladium-N-heterocyclic carbene: A useful catalyst for C-C cross-coupling reaction at ambient condition

A convenient way for the synthesis of benzimidazole-based Pd-N-heterocyclic carbene complex and its structural characterization are described. The complex efficiently catalyzes Suzuki cross-coupling reaction in a wide variety of substrates including heteroaromatic system at ambient condition. The catalyst is also effective for multi Suzuki cross-coupling reaction. In addition, the catalyst is equally active toward C-C cross-coupling reaction between acid chloride and arylboronic acid, giving the desired ketones in high yield.

Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes tuned by gold(i) and silver(i) catalysts: Efficient synthesis of pyran-fused indene cores and 2,4,6-trisubstituted phenols

Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes 1 tuned by gold(i) and silver(i) catalysts are described, which afford selectively the key pyran-fused indene cores 2 and the 2,4,6-trisubstituted phenols 3 in good yields, respectively. The Ro