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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)-

1H-Imidazolium, 1-hexyl-3-methyl-, iodide

CCCCCCN1C=C[NH+](C1)C.[I-] Request for Quotation
Chemical Name: 1H-Imidazolium, 1-hexyl-3-methyl-, iodide
CAS Number: 178631-05-5
Product Number: AG00267D(AGN-PC-0BSL0D)
Synonyms:
MDL No:
Molecular Formula: C10H21IN2
Molecular Weight: 296.1916

Identification/Properties

Computed Properties
Molecular Weight:
294.18g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
5
Exact Mass:
294.059g/mol
Monoisotopic Mass:
294.059g/mol
Topological Polar Surface Area:
8.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
114
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Hexyl-3-methylimidazolium iodide, also known as HMIM-I, is a versatile and efficient ionic liquid that finds application in various chemical synthesis processes. This compound has gained significant interest in the scientific community due to its unique properties and potential in catalysis and organic transformation.Due to its ionic nature, 1-hexyl-3-methylimidazolium iodide serves as an effective reaction medium for a wide range of chemical reactions. It has been utilized as a solvent and catalyst in the synthesis of organic compounds, including organic reactions such as alkylation, acylation, oxidation, and condensation reactions. HMIM-I has shown to enhance reaction rates, selectivity, and yields in many instances, making it a valuable tool for chemists working in the field of synthetic organic chemistry.Moreover, the tunable nature of 1-hexyl-3-methylimidazolium iodide allows for modifications to its structure, providing tailored properties for specific applications. Its ability to dissolve a wide range of organic and inorganic compounds, along with its thermal stability and reusability, further make it a preferred choice in chemical synthesis.In summary, 1-hexyl-3-methylimidazolium iodide is a promising ionic liquid that demonstrates great potential as a versatile solvent and catalyst in various chemical synthesis processes. Its unique properties and versatility make it a valuable asset in the hands of researchers and chemists looking to explore new avenues in synthetic chemistry.