1256355-02-8

Basic information

• Product Name: 4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid
• Synonyms: 4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid
• CAS NO: 1256355-02-8
• Molecular Formula: C10H15BClNO3
• Molecular Weight: 243.495
• Mol File: 1256355-02-8.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Room temperature.
• CAS DataBase Reference: 4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid(1256355-02-8)
• EPA Substance Registry System: 4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid(1256355-02-8)

Safety Data

• Hazardous Substances Data: 1256355-02-8(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid is utilized as a reagent in the Suzuki-Miyaura cross-coupling reaction, a widely employed method for the formation of carbon-carbon bonds. This reaction is crucial for the synthesis of complex organic molecules and contributes to the development of new chemical entities.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid serves as a building block for the synthesis of pharmaceutical compounds. Its unique structure allows for the creation of diverse drug candidates with potential therapeutic applications.
Used in Material Science:
4-Chloro-3-(2-dimethylaminoethoxy)phenylboronic acid may also find applications in material science, particularly in the development of new functional materials. Its properties can be leveraged to design materials with specific characteristics, such as improved conductivity, stability, or reactivity, depending on the intended application.