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56434-29-8

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56434-29-8 Usage

General Description

1,2,4-Triazolo[4,3-b]pyridazine-6-carboxylic acid (9CI) is a chemical compound with the molecular formula C7H4N4O2. It is a heterocyclic compound containing a triazolopyridazine ring system and a carboxylic acid functional group. This chemical is used in the pharmaceutical industry as a building block for the synthesis of potential drug candidates. It has also been studied for its potential biological activities, including antifungal and anticancer properties. The compound's structure and reactivity make it an interesting target for organic synthesis and medicinal chemistry research.

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.

56434-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,2,4]Triazolo[4,3-b]pyridazine-6-carboxylic acid

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

More Details:56434-29-8 SDS

56434-29-8Downstream Products

56434-29-8Relevant articles and documents

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.

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