Product Name:(4-Chloro-3-ethylphenyl)boronic acid
IUPAC Name:(4-chloro-3-ethylphenyl)boronic acid
| Packing Unit | Available Stock | Price($) | Quantity |
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| CM135948-250mg | in stock | ƓǤ |
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| CM135948-1g | in stock | ƥƓȃ |
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| CM135948-5g | in stock | Ǥȃȃ |
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| Product Overview |
(4-Chloro-3-ethylphenyl)boronic acid, also known as CEPBA, is an organic compound belonging to the family of boronic acids. It is a white, crystalline solid with a molecular weight of 184.43 g/mol and a melting point of 164-165°C. CEPBA has a wide range of applications in the scientific and medical fields. It is used as a reagent in organic synthesis and as an active pharmaceutical ingredient (API) in drug development. It has also been used as a catalyst in the preparation of polymers and as a ligand in coordination chemistry. CEPBA is a versatile compound, and its unique properties make it an ideal choice for a variety of applications. |
| Synthesis and Application |
(4-Chloro-3-ethylphenyl)boronic acid can be synthesized by a variety of methods, including the Grignard reaction, the Wittig reaction, and the Ullmann reaction. The Grignard reaction is the most commonly used method for the synthesis of (4-Chloro-3-ethylphenyl)boronic acid. This method involves the reaction of a halogenated alkyl bromide with magnesium metal in the presence of an aprotic solvent such as THF. The reaction produces an intermediate, which is then reacted with a boronic acid to form the desired product. The Wittig reaction involves the reaction of a phosphonium salt with a boronic acid in the presence of a base. Finally, the Ullmann reaction involves the reaction of an alkyl halide with a boronic acid in the presence of a base. (4-Chloro-3-ethylphenyl)boronic acid has a wide range of applications in the scientific and medical fields. It is used as a reagent in organic synthesis and as an active pharmaceutical ingredient (API) in drug development. It has also been used as a catalyst in the preparation of polymers and as a ligand in coordination chemistry. (4-Chloro-3-ethylphenyl)boronic acid has been used in the synthesis of various compounds, including pharmaceuticals, natural products, and polymers. It is also used in the synthesis of small molecules, such as peptides, proteins, and carbohydrates. Additionally, (4-Chloro-3-ethylphenyl)boronic acid has been used in the synthesis of novel materials, such as nanomaterials and nanostructures. |
| Future Directions |
(4-Chloro-3-ethylphenyl)boronic acid has a wide range of potential applications in the scientific and medical fields. It can be used in the synthesis of various compounds, including pharmaceuticals, natural products, and polymers. Additionally, (4-Chloro-3-ethylphenyl)boronic acid can be used in the synthesis of small molecules, such as peptides, proteins, and carbohydrates. (4-Chloro-3-ethylphenyl)boronic acid can also be used in the synthesis of novel materials, such as nanomaterials and nanostructures. Furthermore, (4-Chloro-3-ethylphenyl)boronic acid has potential applications in drug development, as it has been shown to have anti-inflammatory and anti-cancer properties. Finally, (4-Chloro-3-ethylphenyl)boronic acid can be used in the development of new catalysts and ligands for coordination chemistry. |
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