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| CAS number | 400607-46-7 |
| Molecular formula | C24H17BO2 |
| Product name | [10-(1-Naphthalenyl)-9-anthracenyl]boronic acid |
| Molecular Structure |  |
Density：1.3
Boiling Point：574.2ºC at 760 mmHg
Refractive Index：1.767
[10-(1-Naphthalenyl)-9-anthracenyl]boronic acid is a synthetic organic compound with a chemical formula of C21H17BO2. It is a pale yellow solid, soluble in nonpolar organic solvents such as toluene and xylene, but insoluble in water.
The parent compound, 10-(1-naphthalenyl)-9-anthracenylboronic acid, is an important intermediate in the synthesis of dyes, pharmaceuticals and other organic compounds. It has been widely used in the synthesis of a variety of heterocyclic compounds, including dyes, pharmaceuticals, and other organic compounds. In addition, it is also used as a reagent in the synthesis of boronic acid pinacol esters, which are used in the synthesis of highly functionalized organic compounds.
The structure of 10-(1-naphthalenyl)-9-anthracenylboronic acid is composed of a planar naphthyl ring and an anthracene ring attached to it. The naphthyl ring is a cyclic hydrocarbon consisting of two benzene rings fused together, with a single hydrogen atom attached to each ring. The anthracene ring is an aromatic hydrocarbon consisting of three benzene rings fused together, with two hydrogen atoms attached to each ring. The boronic acid group is attached to the anthracene ring, and consists of a boron atom, two oxygen atoms and a hydrogen atom.
The synthesis of 10-(1-naphthalenyl)-9-anthracenylboronic acid is typically achieved through a multi-step process. The first step involves the preparation of the aromatic hydrocarbon, which is achieved by the reaction of a phenol derivative with a boronic acid derivative. The second step involves the coupling of the aromatic hydrocarbon with a 1-naphthol derivative, which produces the desired product.
The properties of 10-(1-naphthalenyl)-9-anthracenylboronic acid are affected by the presence of the naphthyl and anthracene rings. The presence of the naphthyl ring increases the boiling point and decreases the solubility in water, while the presence of the anthracene ring increases the solubility in nonpolar solvents.
The compound has a wide range of applications in organic chemistry. It is used as a building block for the synthesis of a variety of heterocyclic compounds, including dyes, pharmaceuticals, and other organic compounds. It is also used in the synthesis of a variety of boronic acid pinacol esters, which are used in the synthesis of highly functionalized organic compounds. Additionally, it is used as a reagent in the synthesis of a variety of organometallic complexes.
In conclusion, 10-(1-naphthalenyl)-9-anthracenylboronic acid is an important synthetic organic compound with a wide range of applications in organic chemistry. Its structure consists of a planar naphthyl ring and an anthracene ring attached to it, with a boronic acid group attached to the anthracene ring. The properties of this compound are affected by the presence of the naphthyl and anthracene rings, and it is used in the synthesis of a variety of heterocyclic compounds, boronic acid pinacol esters, and organometallic complexes.
