1141889-24-8

Basic information

• Product Name: (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid
• Synonyms: (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid
• CAS NO: 1141889-24-8
• Molecular Formula: C5H10BN3O2
• Molecular Weight: 154.9628
• Mol File: 1141889-24-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
• CAS DataBase Reference: (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid(1141889-24-8)
• EPA Substance Registry System: (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid(1141889-24-8)

Safety Data

• Hazardous Substances Data: 1141889-24-8(Hazardous Substances Data)

Usage

Description

(1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid is a chemical compound with the molecular formula C7H11BN4O2. It is a boronic acid derivative featuring a pyrazole ring and an aminoethyl group. (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid has the potential to serve as a ligand for metal coordination and has been investigated for its medicinal properties, particularly in cancer research. Known for their ability to form stable complexes with diols, boronic acids like this one have been utilized in the development of pharmaceuticals and materials science. The unique structure and properties of (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid position it as a promising building block for synthesizing new chemical compounds with a range of applications across different fields.

Uses

Used in Pharmaceutical Industry:
(1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid is used as a potential medicinal compound for its capacity to act as a ligand in metal coordination. This feature makes it valuable in the development of drugs, particularly in cancer research where its ability to form stable complexes with biological targets can be leveraged for therapeutic purposes.
Used in Materials Science:
In the field of materials science, (1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid is utilized as a building block for the synthesis of new chemical compounds. Its unique structure allows for the creation of materials with diverse properties, contributing to advancements in various applications.
Used in Chemical Synthesis:
(1-(2-Aminoethyl)-1H-pyrazol-4-yl)boronic acid is employed as a synthetic building block in organic chemistry. Its reactivity and functional groups enable the formation of new compounds with potential applications in a wide range of industries, from pharmaceuticals to agrochemicals.