56434-29-8 Usage
Uses
Used in Pharmaceutical Industry:
1,2,4-Triazolo[4,3-b]pyridazine-6-carboxylic acid (9CI) serves as a crucial building block for the synthesis of potential drug candidates, contributing to the discovery of new therapeutic agents with diverse pharmacological profiles.
Used in Organic Synthesis:
1,2,4-Triazolo[4,3-b]pyridazine-6-carboxylicacid(9CI) is employed as a reactive intermediate in organic synthesis, allowing for the creation of a variety of complex molecular structures with potential applications in various fields.
Used in Medicinal Chemistry Research:
1,2,4-Triazolo[4,3-b]pyridazine-6-carboxylic acid (9CI) is utilized in medicinal chemistry research to explore its potential biological activities, such as antifungal and anticancer properties, which could lead to the development of new treatments for various diseases.
Used in Drug Discovery:
1,2,4-Triazolo[4,3-b]pyridazine-6-carboxylicacid(9CI)'s unique structure and reactivity make it an interesting target for drug discovery, where it can be further modified and optimized to enhance its therapeutic potential and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 56434-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56434-29:
(7*5)+(6*6)+(5*4)+(4*3)+(3*4)+(2*2)+(1*9)=128
128 % 10 = 8
So 56434-29-8 is a valid CAS Registry Number.
56434-29-8Relevant academic research and scientific papers
Preparation of Azolopyridazinecarboxylic Acids
Heinisch, G.,Loetsch, G.,Offenberger, S.,Stanovnik, B.,Tisler, M.
, p. 1751 - 1754 (2007/10/02)
Oxidation reactions of various methyl substituted azolopyridazines 2a-d, 3a-h, 4a,b were investigated in order to gain access to the title compounds.This procedure was found to be of limited scope affording only the carboxylic acids 5, 7 and 9.A variety of novel azolopyridazinecarboxylic acid methyl esters bearing one or two methoxycarbonyl groups at the pyridazine core 17,18 and 12,14,16,20, respectively, however, could be prepared by means of a regioselective radical substitution process.
