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1-(3,3-diethoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a chemical compound that features a pyrazole ring fused to a boron-containing group and a diethoxypropyl side chain. The boron-containing group, 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl, is a versatile moiety in organic synthesis, facilitating reactions with other organic molecules to create novel compounds. The diethoxypropyl side chain is a common structural element in the development of pharmaceuticals and agrochemicals, contributing to the compound's potential applications in medicinal chemistry, material science, and agriculture. However, due to the presence of boron, which can be toxic, 1-(3,3-diethoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole must be handled with care in laboratory settings.

847818-73-9

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847818-73-9 Usage

Uses

Used in Medicinal Chemistry:
1-(3,3-diethoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is used as a building block for the synthesis of new pharmaceuticals due to its unique structural features and the reactivity of the boron-containing group, which allows for the formation of new compounds with potential therapeutic properties.
Used in Material Science:
In the field of material science, 1-(3,3-diethoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is used as a precursor for the development of advanced materials, leveraging the versatility of the boron-containing group to create new materials with specific properties.
Used in Agriculture:
1-(3,3-diethoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is used as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides, where the diethoxypropyl side chain can be tailored to target specific biological activities in plants or pests.

Check Digit Verification of cas no

The CAS Registry Mumber 847818-73-9 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, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 847818-73:
(8*8)+(7*4)+(6*7)+(5*8)+(4*1)+(3*8)+(2*7)+(1*3)=219
219 % 10 = 9
So 847818-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H29BN2O4/c1-7-20-14(21-8-2)9-10-19-12-13(11-18-19)17-22-15(3,4)16(5,6)23-17/h11-12,14H,7-10H2,1-6H3

847818-73-9SDS

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-(3,3-diethoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:847818-73-9 SDS

847818-73-9Downstream Products

847818-73-9Relevant academic research and scientific papers

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 (2004)

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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