61070-99-3 Usage
Description
3,6-Pyridazinediamine(9CI), with the molecular formula C4H6N4, is a colorless, crystalline solid that exhibits solubility in organic solvents. This chemical compound is known for its versatility and reactivity, making it a valuable intermediate in the synthesis of a variety of compounds across different industries.
Uses
Used in Pharmaceutical Industry:
3,6-Pyridazinediamine(9CI) is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its reactivity allows for the creation of diverse drug molecules, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 3,6-Pyridazinediamine(9CI) serves as an intermediate in the production of agrochemicals. Its role in synthesizing various compounds aids in the development of pesticides, herbicides, and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Dye Industry:
3,6-Pyridazinediamine(9CI) is utilized as an intermediate in the synthesis of dyes. Its chemical properties enable the production of a range of dyes used in various applications, including textiles, plastics, and printing inks.
Used in Polymer and Resin Production:
3,6-Pyridazinediamine(9CI) is also used as an intermediate in the manufacturing of polymers and resins. Its involvement in the production process contributes to the creation of materials with specific properties required for various applications, such as coatings, adhesives, and composites.
Check Digit Verification of cas no
The CAS Registry Mumber 61070-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,7 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61070-99:
(7*6)+(6*1)+(5*0)+(4*7)+(3*0)+(2*9)+(1*9)=103
103 % 10 = 3
So 61070-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4/c5-3-1-2-4(6)8-7-3/h1-2H,(H2,5,7)(H2,6,8)
61070-99-3Relevant articles and documents
Facile synthesis of 3,6-diaminopyridazine
Xing, Liyan,Petitjean, Anne,Schmidt, Rolf,Cuccia, Louis
, p. 2349 - 2353 (2008/02/09)
An efficient two-step synthesis of 3,6-diaminopyridazine from 3,6-dichloropyridazine is reported. In this synthetic procedure, 4-methoxybenzylamine was used as a nitrogen source to substitute the chloro groups of 3,6-dichloropyridazine to form N,N'-bis-(4-methoxybenzyl)-pyridazine- 3,6-diamine. The 4-methoxybenzyl groups were then removed by treatment with hydrochloric acid to provide the target 3,6-diaminopyridazine with an overall yield of 78%. Copyright Taylor & Francis Group, LLC.
