876442-90-9

876442-90-9 - Names and Identifiers

Name	2-(Phenylnaphthalen-6-yl)boronic acid
Synonyms	6-phenylphthalen-2-yl-2-boronic acid (2-Phenylnaphthalen-6-yl)boronic acid 2-(Phenylnaphthalen-6-yl)boronic acid (6-Phenylnaphthalen-2-yl)boronic acid Boronic acid, (6-phenyl-2-phthalenyl)- -(6-phenyl-2-naphthalenyl) boronic acid B-(6-phenyl-2-naphthalenyl)boronic acid Boronic acid, (6-phenyl-2-naphthalenyl)-
CAS	876442-90-9

876442-90-9 - Physico-chemical Properties

Molecular Formula	C16H13BO2
Molar Mass	248.08
Density	1.23±0.1 g/cm3 (20 ºC 760 Torr)
Boling Point	478.4±43.0 °C(Predicted)
Appearance	Solid
pKa	8.51±0.30(Predicted)
Storage Condition	2-8°C

876442-90-9 - Introduction

2-(Phenylnaphthalen-6-yl)boronic acid is an organic compound with the chemical formula C18H13BO2. It is a white or yellowish solid. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: 2-(Phenylnaphthalen-6-yl)boronic acid appears as a white or yellowish solid, and its form can be crystalline or non-crystalline.
-Solubility: It is soluble in some organic solvents, such as chloroform, benzene and carbon disulfide. However, the solubility in water is relatively low.
-Chemical activity: 2-(Phenylnaphthalen-6-yl)boronic acid is an organic boron compound, commonly used in cross-coupling reactions in organic synthesis reactions. It can participate in the substitution reaction between phenyl and aromatic hydrocarbons to generate new organic compounds.

Use:
- 2-(Phenylnaphthalen-6-yl)boronic acid is an important organic synthesis intermediate, widely used in pharmaceutical synthesis and pesticide synthesis.
-In medicinal chemistry, it is often used to synthesize biologically active molecules, such as drug candidate compounds and fluorescent labeling agents.
-In the field of material science, it can be used as a raw material for organic optoelectronic materials and organic electroluminescent devices.

Preparation Method:
2-(Phenylnaphthalen-6-yl)boronic acid can be synthesized by the reaction of styrene and 2-naphthalene boronic acid. Specific synthetic methods include organometallic reactions, direct chemical bond formation between borides and aromatic compounds, and many other methods.

Safety Information:
- 2-(Phenylnaphthalen-6-yl)boronic acid has low toxicity, but as an organic compound, it may cause certain irritation to the human body. Therefore, appropriate protective measures should be taken during use, such as wearing gloves and breathing apparatus, to avoid direct contact and inhalation.
-When used in a suspended state, avoid dust. Avoid contact with strong oxidants and heat sources to prevent the risk of fire and explosion.
-During storage, it should be stored in a dry, cool place, and avoid contact with acid, alkali and iron to prevent chemical reactions.

Last Update：2024-04-09 20:49:11