Pyridinium, 1,1'-[oxybis(methylene)]bis[4-[(hydroxyimino)methyl]-,dichloride|114-90-9,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)-

Pyridinium, 1,1'-[oxybis(methylene)]bis[4-[(hydroxyimino)methyl]-,dichloride

COC(n1ccc(=C[NH+]=O)cc1)n1ccc(=C[NH+]=O)cc1.[Cl-].[Cl-]

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Chemical Name:	Pyridinium, 1,1'-[oxybis(methylene)]bis[4-[(hydroxyimino)methyl]-,dichloride
CAS Number:	114-90-9
Product Number:	AG008VRY(AGN-PC-0P6XBL)
Synonyms:
MDL No:
Molecular Formula:	C14H16Cl2N4O3
Molecular Weight:	359.2078

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Identification/Properties

Computed Properties

Molecular Weight:

359.207g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

358.06g/mol

Monoisotopic Mass:

358.06g/mol

Topological Polar Surface Area:

82.2A^2

Heavy Atom Count:

Formal Charge:

Complexity:

303

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure

1,1'-(Oxybis(methylene))bis(4-((hydroxyimino)methyl)pyridin-1-ium) chloride is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a crucial reagent for the formation of complex organic structures through various reactions such as condensation, cycloaddition, and functional group transformations. Its ability to act as a bifunctional agent enables it to participate in multiple steps of a synthetic pathway, allowing for efficient and streamlined synthesis of valuable chemical products. Additionally, the unique structural features of this compound, including the presence of pyridinium and hydroxyimino groups, impart specific reactivity patterns that can be harnessed for selective bond formations and functionalization strategies in organic synthesis.