1704069-17-9

Basic information

• Product Name: (4-(1-(diethylaMino)ethyl)phenyl)boronic acid
• Synonyms: (4-(1-(diethylaMino)ethyl)phenyl)boronic acid
• CAS NO: 1704069-17-9
• Molecular Formula: C12H20BNO2
• Molecular Weight: 221.1037
• Mol File: 1704069-17-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 332.6±44.0 °C(Predicted)
• Appearance: /
• Density: 1.04±0.1 g/cm3(Predicted)
• PKA: 8.50±0.17(Predicted)
• CAS DataBase Reference: (4-(1-(diethylaMino)ethyl)phenyl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-(1-(diethylaMino)ethyl)phenyl)boronic acid(1704069-17-9)
• EPA Substance Registry System: (4-(1-(diethylaMino)ethyl)phenyl)boronic acid(1704069-17-9)

Safety Data

• Hazardous Substances Data: 1704069-17-9(Hazardous Substances Data)

Usage

Description

(4-(1-(diethylamino)ethyl)phenyl)boronic acid, also known as DEAB, is a boronic acid derivative that features a phenyl ring with a boronic acid functional group attached to a diethylaminoethyl moiety. This versatile chemical is widely used in various fields, including organic chemistry, biological imaging, and medicinal research.

Uses

Used in Organic Chemistry:
(4-(1-(diethylamino)ethyl)phenyl)boronic acid is used as a reactant in Suzuki coupling reactions, which are crucial for the synthesis of a broad range of organic compounds.
Used in Biological Imaging:
DEAB is employed as a component in the development of fluorescent probes, which are essential for visualizing and studying biological processes at the molecular level.
Used in Catalyst Development:
(4-(1-(diethylamino)ethyl)phenyl)boronic acid serves as a ligand in the creation of novel catalysts for organic reactions, enhancing the efficiency and selectivity of these processes.
Used in Pharmaceutical Research:
DEAB has demonstrated potential as a therapeutic agent for cancer treatment, due to its ability to inhibit the activity of certain enzymes that play a role in cancer progression.
Used in Cancer Therapy:
(4-(1-(diethylamino)ethyl)phenyl)boronic acid is being explored as a potential anticancer agent, targeting enzyme activity crucial for tumor growth and development.