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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-decyl-3-methyl-, chloride

CCCCCCCCCCn1cc[n+](c1)C.[Cl-] Request for Quotation
Chemical Name: 1H-Imidazolium, 1-decyl-3-methyl-, chloride
CAS Number: 171058-18-7
Product Number: AG00HZIR(AGN-PC-0HH9NI)
Synonyms:
MDL No:
Molecular Formula: C14H27ClN2
Molecular Weight: 258.8306

Identification/Properties

Computed Properties
Molecular Weight:
258.834g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
9
Exact Mass:
258.186g/mol
Monoisotopic Mass:
258.186g/mol
Topological Polar Surface Area:
8.8A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
159
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Decyl-3-methylimidazolium chloride is a versatile compound that finds applications in various chemical synthesis processes. As a room-temperature ionic liquid, this substance serves as an efficient solvent and catalyst in organic reactions. Its unique properties allow for enhanced reaction rates and selectivity, making it ideal for conducting a wide range of chemical transformations.In organic synthesis, 1-decyl-3-methylimidazolium chloride can facilitate reactions such as catalytic hydrogenation, metal complexation, and carbon-carbon bond formation. Its solubility characteristics and stability under reaction conditions make it a valuable tool for carrying out challenging transformations with high efficiency.Furthermore, this compound can also be employed in the extraction and purification of organic compounds due to its selective solvation properties. Its ability to dissolve a variety of organic substrates while maintaining good phase separation makes it suitable for applications such as liquid-liquid extraction and separation processes.Overall, 1-decyl-3-methylimidazolium chloride plays a crucial role in modern chemical synthesis by enabling greener and more sustainable reaction pathways with improved yields and reduced environmental impact.