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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-ethyl-3-methylimidazolium dicyanamide

CCn1cc[n+](c1)C.N#CCC#N Request for Quotation
Chemical Name: 1-ethyl-3-methylimidazolium dicyanamide
CAS Number: 923019-22-1
Product Number: AG00H17Q(AGN-PC-0WA4KN)
Synonyms:
MDL No:
Molecular Formula: C9H13N4+
Molecular Weight: 177.2263

Identification/Properties

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


1-Ethyl-3-methylimidazolium dicyanomethanide, a versatile ionic liquid, serves as a crucial reagent in modern chemical synthesis. This unique compound, due to its ionic nature and exceptional solubility properties, significantly enhances the efficiency and yield of various chemical reactions. In chemical synthesis, 1-Ethyl-3-methylimidazolium dicyanomethanide functions as a potent catalyst, enabling the activation of otherwise inert substrates and facilitating the formation of complex molecular structures. Its ability to dissolve a wide range of organic and inorganic compounds makes it an ideal medium for conducting reactions involving insoluble or unstable reactants.Moreover, the presence of the dicyanomethanide anion in this ionic liquid imparts nucleophilic character, enabling it to participate in various nucleophilic substitution reactions and contribute to the synthesis of novel compounds. Additionally, the imidazolium cation provides stability and control over the reaction conditions, ensuring reproducibility and scalability in chemical transformations.Overall, the application of 1-Ethyl-3-methylimidazolium dicyanomethanide in chemical synthesis exemplifies its pivotal role in modern organic chemistry by enabling the efficient and sustainable production of complex molecules with high purity and yield.