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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, 1-butyl-, chloride

CCCC[n+]1ccccc1.[Cl-] Request for Quotation
Chemical Name: Pyridinium, 1-butyl-, chloride
CAS Number: 1124-64-7
Product Number: AG003E6R(AGN-PC-00UNW8)
Synonyms:
MDL No:
Molecular Formula: C9H14ClN
Molecular Weight: 171.6672

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
171.668g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
171.081g/mol
Monoisotopic Mass:
171.081g/mol
Topological Polar Surface Area:
3.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
74.8
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-Butylpyridinium Chloride (1-BuPyCl) offers a unique application in chemical synthesis as a versatile and efficient phase transfer catalyst. With its quaternary ammonium structure, this compound effectively facilitates the transfer of ions or molecules between immiscible phases, enabling reactions that would otherwise be challenging or impossible.In organic synthesis, 1-Butylpyridinium Chloride enhances the solubility of reactants in different phases, promoting efficient reaction conditions and increasing reaction yields. It is particularly useful in reactions involving nucleophilic substitution, alkylation, and esterification. Additionally, this compound can catalyze reactions that require the activation of typically unreactive species, making it a valuable tool in complex synthesis strategies.Furthermore, 1-Butylpyridinium Chloride's stability and compatibility with a wide range of reaction conditions make it an excellent choice for chemists working on various synthetic methodologies. Its ability to accelerate reactions, improve selectivity, and simplify reaction procedures highlight its importance in the realm of chemical synthesis.