663954-31-2

Basic information

• Product Name: 2-P-TERPHENYLBORONIC ACID
• Synonyms: 2-P-TERPHENYLBORONIC ACID;2-p-Terphenylboronic Acid (contains varying amounts of Anhydride);2-(4-Biphenyl)phenyl boronic acid;2-p-Terphenylboronic Acid 2- p-terphenylbirinic acid;[1,1':4',1''-Terphenyl]-2-ylboronic acid
• CAS NO: 663954-31-2
• Molecular Formula: C₁₈H₁₅BO₂
• Molecular Weight: 274.13
• Product Categories: B (Classes of Boron Compounds);Boronic Acids;Boronic acid series
• Mol File: 663954-31-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 522.595 °C at 760 mmHg
• Flash Point: 269.856 °C
• Appearance: /
• Density: 1.211 g/cm³
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: soluble in Tetrahydrofuran
• PKA: 8.55±0.58(Predicted)
• CAS DataBase Reference: 2-P-TERPHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-P-TERPHENYLBORONIC ACID(663954-31-2)
• EPA Substance Registry System: 2-P-TERPHENYLBORONIC ACID(663954-31-2)

Safety Data

• Hazardous Substances Data: 663954-31-2(Hazardous Substances Data)

Usage

General Description

2-P-Terphenylboronic acid is a chemical compound with the molecular formula C18H15BO2. It is a boronic acid derivative that contains a boron atom bonded to three oxygen atoms. 2-P-TERPHENYLBORONIC ACID is commonly used in organic synthesis and catalysis as a reagent for the Suzuki-Miyaura cross-coupling reaction, which is a widely used method for the formation of carbon-carbon bonds. It has also been studied for its potential use in the development of new materials and pharmaceuticals. Additionally, 2-P-Terphenylboronic acid is known for its fluorescent properties, making it useful in fluorescence-based detection methods. Overall, this compound plays a significant role in the field of organic chemistry and has a range of potential applications in various industries.

Upstream product

• 121-43-7 Trimethyl borate 
• 3282-24-4 2-bromo-[1,1';4',1]terphenyl 
• 7732-18-5 water 

Relevant articles and documents

Rh(III)-Catalyzed C-H Activation of Boronic Acid with Aryl Azide

A Rh(III)-catalyzed C-H activation of boronic acid with aryl azide to obtain unsymmetric carbazoles, 1H-indoles, or indolines has been developed. The reaction constructs dual distinct C-N bonds via sp2/sp3 C-H activation and rhodium nitrene insertion. Synthetically, this approach represents an access to widely used carbazole derivatives. The practical application to CBP and unsymmetric TCTA derivatives has also been performed. Mechanistic experiments and DFT calculations demonstrate that a five-membered rhodacycle species is the key intermediate.