(6-methoxypyrazin-2-yl)hydrazine|954227-93-1,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-methoxypyrazin-2-yl)hydrazine

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Chemical Name:	(6-methoxypyrazin-2-yl)hydrazine
CAS Number:	954227-93-1
Product Number:	AG0060AO(AGN-PC-01XQC5)
Synonyms:
MDL No:
Molecular Formula:	C5H8N4O
Molecular Weight:	140.1432

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Identification/Properties

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Keep in dry area;2-8℃;

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Chemical Structure

2-Hydrazinyl-6-methoxypyrazine, a versatile chemical compound, finds a pivotal role in chemical synthesis as a key building block. This compound is renowned for its unparalleled ability to act as a reliable precursor in the synthesis of various biologically active molecules and pharmaceutical intermediates. With its unique structure and highly reactive hydrazine and methoxy functional groups, 2-Hydrazinyl-6-methoxypyrazine serves as a potent reagent in the creation of complex organic compounds through nucleophilic addition and substitution reactions. Harnessing its synthetic potential, researchers exploit this compound to facilitate the construction of novel drug candidates, agrochemicals, and functional materials, underscoring its significance in modern organic synthesis strategies.