1704074-48-5

Basic information

• Product Name: (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid
• Synonyms: (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid
• CAS NO: 1704074-48-5
• Molecular Formula: C13H20BClN2O2
• Molecular Weight: 282.5741
• Mol File: 1704074-48-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid(1704074-48-5)
• EPA Substance Registry System: (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid(1704074-48-5)

Safety Data

• Hazardous Substances Data: 1704074-48-5(Hazardous Substances Data)

Usage

Description

(4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid is a boronic acid derivative characterized by its molecular formula C14H22BClN2O2. (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid is recognized for its structural complexity and potential reactivity, making it a valuable tool in the synthesis of new chemical entities. Its unique structure, which includes a piperazine group, suggests possible biological activity and the ability to interact with biological targets, positioning it as a promising candidate for pharmaceutical development and chemical research.

Uses

Used in Chemical Research:
(4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid is used as a reagent in chemical research for the synthesis of various organic compounds. Its versatile nature allows for the creation of a wide range of chemical entities, contributing to the advancement of the field.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid is utilized as a building block for the development of new drugs. The presence of the piperazine group indicates potential interactions with biological targets, which can be harnessed for therapeutic purposes.
Used in Medicinal Chemistry:
(4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid is employed as a key component in medicinal chemistry due to its ability to form stable covalent bonds with diols. This property is particularly useful in the design and synthesis of bioactive molecules with potential applications in treating various diseases and conditions.
Used in Material Science:
(4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid is also used in material science, where its structural properties and reactivity can be leveraged to develop new materials with specific characteristics and applications. The versatility of (4-chloro-3-((4-ethylpiperazin-1-yl)Methyl)phenyl)boronic acid makes it an important asset in the field of material science, contributing to the development of innovative materials with diverse uses.