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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)-

methyl sulfate;tributyl(methyl)azanium

COS(=O)(=O)[O-].CCCC[N+](CCCC)(CCCC)C Request for Quotation
Chemical Name: methyl sulfate;tributyl(methyl)azanium
CAS Number: 13106-24-6
Product Number: AG000VGV(AGN-PC-0NEYXS)
Synonyms:
MDL No:
Molecular Formula: C14H33NO4S
Molecular Weight: 311.4811

Identification/Properties

Computed Properties
Molecular Weight:
311.48g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
9
Exact Mass:
311.21303g/mol
Monoisotopic Mass:
311.21303g/mol
Topological Polar Surface Area:
74.8Ų
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
189
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


Tributylmethylammonium methyl sulfate is a versatile chemical compound commonly used in chemical synthesis processes. This compound functions as a phase-transfer catalyst, facilitating the transfer of reactants between immiscible phases such as aqueous and organic solvents. By acting as a mediator between these phases, Tributylmethylammonium methyl sulfate promotes efficient reactions by increasing the solubility of reactants and enhancing the interaction between them.In chemical synthesis, this compound is particularly valued for its ability to accelerate reactions that would otherwise be slow or inefficient under normal conditions. It can aid in various reactions including alkylation, esterification, and Michael additions, among others. Additionally, Tributylmethylammonium methyl sulfate is known for its high selectivity and tolerance towards a wide range of functional groups, making it a preferred choice in complex synthesis routes where maintaining specificity is crucial.Moreover, this compound is known for its ease of handling and stability, ensuring consistent and reliable results in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its compatibility with a diverse array of substrates and reaction conditions further expands its utility in the chemical industry, where precise control over reaction parameters is essential for the successful production of target compounds.