6-Chloro-N3-methylpyridazine-3,4-diamine|17645-17-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

6-Chloro-N3-methylpyridazine-3,4-diamine

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Chemical Name:	6-Chloro-N3-methylpyridazine-3,4-diamine
CAS Number:	17645-17-9
Product Number:	AG0024PB(AGN-PC-0WAMGC)
Synonyms:
MDL No:	MFCD20672395
Molecular Formula:	C5H7ClN4
Molecular Weight:	158.5889

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Chemical Structure

6-Chloro-N3-methylpyridazine-3,4-diamine, a versatile chemical compound, serves as a crucial building block in organic synthesis. It plays a pivotal role in the development of pharmaceuticals, agrochemicals, and materials science. With its unique structure and reactivity, this compound is widely utilized in the preparation of complex molecules through various synthetic routes. Its presence enhances the efficacy and selectivity of certain reactions, making it an indispensable tool for organic chemists. Moreover, 6-Chloro-N3-methylpyridazine-3,4-diamine offers the opportunity for structural modifications and derivatization, enabling the creation of novel compounds with enhanced properties and functions. Its application in chemical synthesis extends across different fields, highlighting its significance in advancing scientific research and innovation.