1704073-39-1

Basic information

• Product Name: (4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride
• Synonyms: (4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride
• CAS NO: 1704073-39-1
• Molecular Formula: C11H17BClNO2
• Molecular Weight: 241.52218
• Mol File: 1704073-39-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride(1704073-39-1)
• EPA Substance Registry System: (4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride(1704073-39-1)

Safety Data

• Hazardous Substances Data: 1704073-39-1(Hazardous Substances Data)

Usage

Description

(4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride is a boronic acid derivative featuring a cyclopropylamino group. It is known for its ability to form covalent bonds with diols and other nucleophilic functional groups, making it a versatile compound in organic synthesis and pharmaceutical research. The hydrochloride salt form enhances its solubility in water, which is beneficial for biological assays and experiments.

Uses

Used in Organic Synthesis:
(4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride is used as a synthetic building block for creating a variety of complex organic molecules. Its ability to form covalent bonds with diols and other nucleophilic functional groups allows for the development of novel chemical structures with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride is used as a key intermediate in the development of new drugs. Its unique reactivity and functional group compatibility make it a valuable compound for designing and synthesizing potential therapeutic agents.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
(4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride is utilized as a coupling partner in Suzuki-Miyaura cross-coupling reactions with aryl halides. This reaction is a powerful tool in organic chemistry for forming carbon-carbon bonds, which are essential in the synthesis of many biologically active compounds and advanced materials.
Used in Drug Development:
(4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride has potential applications in the development of new drugs, particularly due to its reactivity and compatibility with various functional groups. Its ability to form stable covalent bonds with biologically relevant molecules makes it a promising candidate for the creation of novel therapeutic agents.
Used in Material Science:
(4-(1-(cyclopropylaMino)ethyl)phenyl)boronic acid hydrochloride can also be employed in the development of new materials, such as polymers and coatings, that may have unique properties due to the presence of the boronic acid functionality and the cyclopropylamino group.