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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)-

Benzenemethanaminium, N,N-dimethyl-N-phenyl-, chloride

C[N+](c1ccccc1)(Cc1ccccc1)C.[Cl-] Request for Quotation
Chemical Name: Benzenemethanaminium, N,N-dimethyl-N-phenyl-, chloride
CAS Number: 3204-68-0
Product Number: AG003O4V(AGN-PC-0JLQ6N)
Synonyms:
MDL No:
Molecular Formula: C15H18ClN
Molecular Weight: 247.7631

Identification/Properties

Properties
MP:
134-138°C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
247.766g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
247.113g/mol
Monoisotopic Mass:
247.113g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
198
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:
Danger
UN#:
3077
Hazard Statements:
H302-H314-H317-H400
Precautionary Statements:
P273-P280-P305+P351+P338-P310
Class:
9
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Benzyl-N,N-dimethylbenzenaminium chloride, also known as Benzyltrimethylammonium chloride, is a versatile compound widely used in chemical synthesis as a phase transfer catalyst. This quaternary ammonium salt acts as a catalyst by facilitating the transfer of reactants between two immiscible phases, typically an organic and an aqueous phase. Its application in chemical synthesis allows for improved reaction efficiencies and selectivities, especially in reactions involving nucleophilic substitutions, oxidations, and alkylations. The unique properties of N-Benzyl-N,N-dimethylbenzenaminium chloride make it an essential component in synthetic chemistry, enabling the synthesis of a wide range of organic compounds with high yields and purity.