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Pyridazine-4-boronic acid pinacol ester is a chemical compound that belongs to the class of boronic acids and esters. It is characterized by a molecular formula of C12H18BNO2 and features a pyridazine ring, which is a heterocyclic compound with two nitrogen atoms. This substance is commonly found in its solid form and is used as a reagent in the synthesis of various compounds, particularly in the field of organic chemistry.

863422-41-7

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863422-41-7 Usage

Uses

Used in Organic Chemistry Research:
Pyridazine-4-boronic acid pinacol ester is used as a reagent for the synthesis of various compounds in organic chemistry. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable tool in the development of new molecules and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, pyridazine-4-boronic acid pinacol ester is used as a building block for the synthesis of potential drug candidates. Its ability to form stable intermediates and participate in complex reactions enables the creation of novel molecules with potential therapeutic applications.
Used in Material Science:
Pyridazine-4-boronic acid pinacol ester is also utilized in material science for the development of new materials with specific properties. Its versatility in forming chemical bonds and its stability make it a suitable candidate for the synthesis of advanced materials with applications in various fields, such as electronics, energy storage, and sensors.

Check Digit Verification of cas no

The CAS Registry Mumber 863422-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,4,2 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 863422-41:
(8*8)+(7*6)+(6*3)+(5*4)+(4*2)+(3*2)+(2*4)+(1*1)=167
167 % 10 = 7
So 863422-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15BN2O2/c1-9(2)10(3,4)15-11(14-9)8-5-6-12-13-7-8/h5-7H,1-4H3

863422-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridazine

1.2 Other means of identification

Product number -
Other names Pyridazin-4-boronic acid pinacol ester

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:863422-41-7 SDS

863422-41-7Downstream Products

863422-41-7Relevant academic research and scientific papers

Synthesis of highly substituted pyridazines through alkynyl boronic ester cycloaddition reactions

Helm, Matthew D.,Moore, Jane E.,Plant, Andrew,Harrity, Joseph P. A.

, p. 3889 - 3892 (2005)

(Chemical Equation Presented) A highly regioselective transformation of tetrazines through a cycloaddition reaction with alkynyl boronic esters provides highly substituted pyridazine boronic esters as intermediates for C-O and C-C bond-forming reactions (see scheme). Functionalization reactions of the C-B bond, such as oxidation and the Suzuki cross-coupling, show the versatility of these species.

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