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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)-

3-Iodobenzylguanidinium-sulfate

OS(=O)(=O)O.Ic1cccc(c1)C[NH2+]C(=N)N Request for Quotation
Chemical Name: 3-Iodobenzylguanidinium-sulfate
CAS Number: 103346-16-3
Product Number: AG008T1D(AGN-PC-0NVKCF)
Synonyms:
MDL No:
Molecular Formula: C8H13IN3O4S+
Molecular Weight: 374.17599

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Chemical Structure


Guanidine, N-[(3-iodophenyl)methyl]-, sulfate is a versatile reagent widely used in chemical synthesis for its unique properties and applications. This compound is particularly valuable in organic chemistry as a powerful nucleophilic reagent due to the highly electrophilic nature of the iodine atom. In the field of chemical synthesis, Guanidine, N-[(3-iodophenyl)methyl]-, sulfate is commonly employed in the preparation of various pharmaceutical intermediates and complex organic molecules. Its ability to undergo nucleophilic substitution reactions makes it a valuable tool for the introduction of the iodophenylmethyl group into target molecules.Furthermore, the sulfate counterion in this compound enhances its solubility in polar solvents, facilitating its use in a wide range of synthetic transformations. Whether it is used in coupling reactions, cross-coupling reactions, or other carbon-carbon bond forming reactions, Guanidine, N-[(3-iodophenyl)methyl]-, sulfate plays a crucial role in the efficient synthesis of organic compounds with diverse applications.