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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)-

4-Pyridinamine, N,N-dimethyl-, mono(4-methylbenzenesulfonate)

CN(c1ccncc1)C.Cc1ccc(cc1)S(=O)(=O)O Request for Quotation
Chemical Name: 4-Pyridinamine, N,N-dimethyl-, mono(4-methylbenzenesulfonate)
CAS Number: 91944-64-8
Product Number: AG00IGYO(AGN-PC-0VXFUF)
Synonyms:
MDL No:
Molecular Formula: C14H18N2O3S
Molecular Weight: 294.3693

Identification/Properties

Computed Properties
Molecular Weight:
294.369g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
294.104g/mol
Monoisotopic Mass:
294.104g/mol
Topological Polar Surface Area:
78.9A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
281
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N-Dimethylpyridin-4-amine 4-methylbenzenesulfonate is a versatile compound commonly used in chemical synthesis. 
It serves as an efficient catalyst in various organic reactions, particularly in the formation of carbon-carbon and carbon-nitrogen bonds. 
Due to its unique structure, this compound facilitates the activation of certain functional groups and promotes the desired chemical transformations with high selectivity and yield. 
In addition, N,N-Dimethylpyridin-4-amine 4-methylbenzenesulfonate is valued for its ability to accelerate reactions under mild conditions, making it a valuable tool in the synthesis of complex molecules in pharmaceutical, agrochemical, and material science industries.