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1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan is a versatile chemical compound utilized in the realms of organic synthesis and material science. It features a propyl group connected to a boron atom, which is in turn bonded to a tetramethyl-1,3,2-dioxaborolan ring. 1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan is recognized for its high stability and compatibility with a broad spectrum of reagents and solvents, establishing it as a crucial reagent in organic reactions and a precursor for the synthesis of diverse materials, including polymers and pharmaceuticals. Its distinctive structure and attributes render it an advantageous building block for the creation of innovative chemical compounds tailored for a multitude of industrial and scientific applications.

847818-76-2

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847818-76-2 Usage

Uses

Used in Organic Synthesis:
1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Material Science:
In the field of material science, 1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan is used as a precursor to synthesize a range of materials, such as polymers and pharmaceuticals, due to its unique structural properties that allow for the development of novel material compositions.
Used in Pharmaceutical Industry:
1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan is employed as a building block in the pharmaceutical industry for the development of new drugs, leveraging its compatibility with other reagents to create molecules with potential therapeutic applications.
Used in Polymer Industry:
Within the polymer industry, 1-Propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan is utilized as a component in the synthesis of polymers, taking advantage of its structural attributes to engineer polymers with specific properties for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 847818-76-2 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 847818-76:
(8*8)+(7*4)+(6*7)+(5*8)+(4*1)+(3*8)+(2*7)+(1*6)=222
222 % 10 = 2
So 847818-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H21BN2O2/c1-6-9-15-10(7-8-14-15)13-16-11(2,3)12(4,5)17-13/h7-8H,6,9H2,1-5H3

847818-76-2SDS

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

1.2 Other means of identification

Product number -
Other names 1-propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole

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:847818-76-2 SDS

847818-76-2Downstream Products

847818-76-2Relevant 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 (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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