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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

1-(Pyridin-4-yl)guanidine

NC(=N)Nc1ccncc1 Request for Quotation
Chemical Name: 1-(Pyridin-4-yl)guanidine
CAS Number: 425376-94-9
Product Number: AG00CLYS(AGN-PC-0WAI0B)
Synonyms:
MDL No:
Molecular Formula: C6H8N4
Molecular Weight: 136.15452

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Pyridin-4-yl)guanidine, a versatile organic compound, finds significant application in chemical synthesis as a potent building block for the construction of various pharmaceuticals and fine chemicals. With its unique structure featuring a pyridine ring fused to a guanidine moiety, this compound offers a wide range of reactivity and functional group compatibility.In synthetic chemistry, 1-(Pyridin-4-yl)guanidine serves as a valuable intermediate for the preparation of diverse heterocyclic compounds, including pyrimidines, triazines, and pyrazoles. Its ability to undergo various transformations such as alkylation, acylation, and cyclization makes it indispensable in the synthesis of biologically active molecules.Furthermore, the presence of both nitrogen-based functionalities in 1-(Pyridin-4-yl)guanidine allows for the introduction of pharmacophores and tuning of the compound's physicochemical properties, making it a key component in the design and development of novel drug candidates. Its versatility and reactivity make it a sought-after reagent in the pharmaceutical industry and academic research for the creation of structurally diverse compounds with potential therapeutic applications.