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1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID is a chemical compound characterized by the presence of a boronic acid functional group and a pyrazole ring. 1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID is recognized for its versatility in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The boronic acid group's ability to form stable complexes with diols makes it a key player in numerous cross-coupling reactions. The 1-propyl substituent on the pyrazole ring enhances the compound's complexity and adaptability, facilitating the customization of its chemical properties. As such, 1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID serves as an indispensable building block in the creation of biologically active molecules and functional materials.

847818-57-9

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847818-57-9 Usage

Uses

Used in Pharmaceutical Synthesis:
1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID is used as a reagent in the synthesis of various pharmaceutical compounds due to its ability to participate in cross-coupling reactions, which are essential for constructing complex molecular structures with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID is utilized as a precursor in the development of agrochemicals, leveraging its reactivity in organic synthesis to create compounds that can be used in crop protection and other agricultural applications.
Used in Organic Synthesis Research:
1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID is employed as a research tool in organic synthesis, where its unique structural features allow chemists to explore new reaction pathways and develop innovative synthetic methods for creating novel molecules with specific properties.
Used in the Development of Functional Materials:
1-PROPYL-1H-PYRAZOL-4-YLBORONIC ACID is also used as a building block in the synthesis of functional materials, where its boronic acid group and pyrazole ring can be tailored to create materials with specialized properties for applications in various industries, such as sensors, catalysts, or advanced materials for energy storage and conversion.

Check Digit Verification of cas no

The CAS Registry Mumber 847818-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,8,1 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 847818-57:
(8*8)+(7*4)+(6*7)+(5*8)+(4*1)+(3*8)+(2*5)+(1*7)=219
219 % 10 = 9
So 847818-57-9 is a valid CAS Registry Number.

847818-57-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-Propyl-1H-pyrazol-4-yl)boronic acid

1.2 Other means of identification

Product number -
Other names (1-propylpyrazol-4-yl)boronic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:847818-57-9 SDS

847818-57-9Relevant academic research and scientific papers

NURR1 RECEPTOR MODULATORS

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Paragraph 0646; 0838-0840, (2020/09/08)

Described herein, inter alia, are Nurr1 receptor modulators and uses thereof. In an aspect is provided a method for treating a disease associated with dysregulation and/or degeneration of dopaminergic neurons in the central nervous system of a subject in need thereof, the method including administering to the subject in need thereof a therapeutically effective amount of a compound described herein.

Synthesis of pinacol esters of 1-alkyl-1H-pyrazol-5-yl- and 1-alkyl-1H-pyrazol-4-ylboronic acids

Ivachtchenko, Alexandre V.,Kravchenko, Dmitry V.,Zheludeva, Valentina I.,Pershin, Dmitry G.

, p. 931 - 939 (2007/10/03)

Starting from 1H-pyrazol, a wide number of 1-alkyl-1H-pyrazol-4-yl and 1-alkyl-1H-pyrazol-5-ylboronic acids and their pinacol esters were synthesized and characterized. The key step in the described methodology is the regioselective lithiation of the pyrazole ring. The synthesized pinacolates are stable under prolonged storage and can be used as convenient reagents in organic synthesis.

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