1086063-73-1

Basic information

• Product Name: (1-(2-(Dimethylamino)ethyl)-1H-pyrazol-4-yl)boronic acid
• Synonyms: (1-(2-(Dimethylamino)ethyl)-1H-pyrazol-4-yl)boronic acid;B-[1-[2-(dimethylamino)ethyl]-1H-pyrazol-4-yl]boronic acid
• CAS NO: 1086063-73-1
• Molecular Formula: C7H14BN3O2
• Molecular Weight: 183.01596
• Mol File: 1086063-73-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 349.9±48.0 °C(Predicted)
• Appearance: /
• Density: 1.13±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 7.05±0.10(Predicted)
• CAS DataBase Reference: (1-(2-(Dimethylamino)ethyl)-1H-pyrazol-4-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(2-(Dimethylamino)ethyl)-1H-pyrazol-4-yl)boronic acid(1086063-73-1)
• EPA Substance Registry System: (1-(2-(Dimethylamino)ethyl)-1H-pyrazol-4-yl)boronic acid(1086063-73-1)

Safety Data

• Hazardous Substances Data: 1086063-73-1(Hazardous Substances Data)

Usage

Description

(1-(2-(Dimethylamino)ethyl)-1H-pyrazol-4-yl)boronic acid, also known as DMAPB, is a boronic acid derivative that features a pyrazole ring and a dimethylaminoethyl group. This versatile chemical is widely recognized for its applications in various fields of chemistry and biology, including organic synthesis, pharmaceutical development, and material science.
Used in Pharmaceutical Industry:
DMAPB is utilized as a reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal for creating carbon-carbon bonds essential in the synthesis of pharmaceuticals. Its role in these reactions contributes to the development of new and improved medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, DMAPB serves as a key reagent in cross-coupling reactions that facilitate the production of agrochemicals, thereby playing a role in the development of pesticides and other agricultural products.
Used in Organic Material Production:
DMAPB is also used in the synthesis of organic materials, where its participation in cross-coupling reactions aids in the creation of advanced materials with specific properties for various applications.
Used in Cancer Research:
DMAPB has been studied for its potential as an anti-cancer compound, demonstrating the ability to inhibit the growth of cancer cells in vitro. This research indicates its possible use in the development of new cancer treatments.
Used in Analytical Chemistry:
The development of fluorescent sensors for detecting metal ions benefits from DMAPB's properties, making it a component in analytical chemistry for sensitive and selective detection methods.
Used in Catalysis and Material Science:
DMAPB contributes to the preparation of functionalized materials that find applications in catalysis and material science, further expanding its utility across different scientific disciplines.