1072945-81-3

Basic information

• Product Name: 1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-ylboronic acid
• CAS NO: 1072945-81-3
• Molecular Formula: C7H6BClN4O2
• Molecular Weight: 224.41214
• Mol File: 1072945-81-3.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-ylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-ylboronic acid(1072945-81-3)
• EPA Substance Registry System: 1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-ylboronic acid(1072945-81-3)

Safety Data

• Hazardous Substances Data: 1072945-81-3(Hazardous Substances Data)

Usage

Description

(1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-yl)boronic acid is a versatile chemical compound characterized by the presence of a boronic acid group attached to a pyrazole ring, which is further substituted with a chloropyrimidine group. This unique structure endows the compound with high reactivity and the ability to form covalent bonds with other organic molecules, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.

Uses

Used in Pharmaceutical Synthesis:
(1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-yl)boronic acid is used as a key building block in the development of novel pharmaceuticals. Its reactivity and ability to form covalent bonds with other organic molecules allow for the creation of new chemical entities with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, (1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-yl)boronic acid serves as an essential component in the synthesis of various agrochemicals. Its unique structure and reactivity contribute to the development of innovative products with improved efficacy and selectivity in crop protection.
Used in Medicinal Chemistry Research:
(1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-yl)boronic acid is employed as a valuable tool in medicinal chemistry research. Its versatility in organic synthesis enables the exploration of new chemical space and the identification of potential drug candidates with novel pharmacological activities.
Overall, the unique structure and reactivity of (1-(6-Chloropyrimidin-4-yl)-1H-pyrazol-4-yl)boronic acid make it a promising compound for various applications across different industries, including pharmaceuticals, agrochemicals, and medicinal chemistry research. Its ability to form covalent bonds with other organic molecules and its potential to create new chemical entities with therapeutic applications highlight its significance in the development of innovative products and drug candidates.