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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)-

Pyridinium, 2-[(hydroxyimino)methyl]-1-methyl-, iodide

O/N=C/c1cccc[n+]1C.[I-] Request for Quotation
Chemical Name: Pyridinium, 2-[(hydroxyimino)methyl]-1-methyl-, iodide
CAS Number: 94-63-3
Product Number: AG003HX1(AGN-PC-0ONX7F)
Synonyms:
MDL No:
Molecular Formula: C7H9IN2O
Molecular Weight: 264.0636

Identification/Properties

Properties
MP:
220 °C (dec.)(lit.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Light Sensitive

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Hydroximinomethyl)-1-methylpyridinium iodide serves as a versatile reagent in various chemical synthesis reactions. This compound is commonly employed as a powerful catalyst in organic transformations, particularly in the formation of new carbon-carbon or carbon-nitrogen bonds. Its functionality as a halonium ion surrogate enables the efficient activation of nucleophiles, leading to the creation of complex molecular structures. Additionally, 2-(Hydroximinomethyl)-1-methylpyridinium iodide facilitates the selective modification of functional groups within organic molecules, offering a valuable tool for chemists seeking to enhance the regio- and stereoselectivity of their synthetic routes. Whether employed in the construction of natural products or the design of novel pharmaceutical intermediates, this reagent plays a crucial role in advancing the field of chemical synthesis.