870774-29-1

Basic information

• Product Name: 3-(naphthalene-2-yl)phenylboronic acid
• Synonyms: 3-(naphthalene-2-yl)phenylboronic acid;[3-(2-Naphthalenyl)phenyl]boronic acid;(3-(Naphthalen-2-yl)phenyl)boronic acid;B-[3-(2-naphthalenyl)phenyl]Boronic acid;3-(2-Naphthyl)phenylboronic Acid (contains varying amounts of Anhydride);(3-(Naphthalen-2-yl)
• CAS NO: 870774-29-1
• Molecular Formula: C₁₆H₁₃BO₂
• Molecular Weight: 248.08422
• Mol File: 870774-29-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 486.0±48.0 °C(Predicted)
• Appearance: /
• Density: 1.23±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.27±0.19(Predicted)
• CAS DataBase Reference: 3-(naphthalene-2-yl)phenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(naphthalene-2-yl)phenylboronic acid(870774-29-1)
• EPA Substance Registry System: 3-(naphthalene-2-yl)phenylboronic acid(870774-29-1)

Safety Data

• Hazardous Substances Data: 870774-29-1(Hazardous Substances Data)

Usage

General Description

3-(naphthalene-2-yl)phenylboronic acid is a compound with the chemical formula C16H13BO2. It is a boronic acid derivative, which contains a phenyl group attached to the boron atom with a naphthalene ring as a substituent. 3-(naphthalene-2-yl)phenylboronic acid is commonly used in organic synthesis as a reagent for the Suzuki coupling reaction, a widely employed method for the formation of carbon-carbon bonds. It is also utilized in the development of materials such as organic light-emitting diodes (OLEDs) and pharmaceuticals due to its ability to form stable complexes with various substrates. Overall, 3-(naphthalene-2-yl)phenylboronic acid plays a crucial role in the field of organic chemistry and materials science.

Upstream product

• 32316-92-0 naphthalene-2-boronic acid 
• 667940-23-0 2-(3-bromophenyl)naphthalene 
• 5419-55-6 Triisopropyl borate 

Downstream Products

• 944801-33-6 9-bromo-10-(3-(naphthalen-2-yl)phenyl)anthracene 

Relevant articles and documents

Scyllo-inositol as a convenient protecting group for aryl boronic acids in Suzuki-Miyaura cross-coupling reactions

Herein, we report air-and water-stable borate complexes between scyllo-inositol and aryl boronic acids. The complexes were less reactive than free aryl boronic acids under Suzuki-Miyaura cross-coupling reaction conditions; thus, the borate complexes were used as protected boronic acids. Although protecting groups for organoboronic acids are useful in coupling reactions, especially those used to produce π-conjugated molecules, only a few reports describing the use of protecting groups for boronic acids have been published. The proposed unique structural borate complex provides a novel protective method for aryl boronic acids.

NAPHTHALENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE DEVICE, AND ORGANIC ELECTROLUMINESCENCE DEVICE USING THE SAME

A naphthalene derivative represented by the following formula (1) is provided. In the formula, Ar1 to Ar4 each represent an aromatic hydrocarbon cyclic group having 6 to 18 carbon atoms forming a ring. The aromatic hydrocarbon cyclic group has none of anthracene skeleton, pyrene skeleton, aceanthrylene skeleton and naphthacene skeleton. n, m and 1 each represent an integer in a range of 1 to 5. p represents an integer in a range of o to 5. When n, m, 1 and p each are 2 or more, a plurality of Ar1 to Ar4 may be mutually the same or different.