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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)-

1,4-Benzenediamine, N4,N4,2-trimethyl-

CN(c1ccc(c(c1)C)N)C Request for Quotation
Chemical Name: 1,4-Benzenediamine, N4,N4,2-trimethyl-
CAS Number: 2359-53-7
Product Number: AG002NTC(AGN-PC-0MTZ1A)
Synonyms:
MDL No:
Molecular Formula: C9H14N2
Molecular Weight: 150.2209

Identification/Properties

Computed Properties
Molecular Weight:
150.225g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
150.116g/mol
Monoisotopic Mass:
150.116g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
123
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N1,N1,3-Trimethylbenzene-1,4-diamine, also known as TMEDA, is a versatile compound widely used in chemical synthesis as a ligand in various metal-catalyzed reactions. Its unique structure and properties make it a valuable tool in organic chemistry applications.In complexation reactions, TMEDA can coordinate with transition metals to form stable complexes that facilitate a wide range of catalytic reactions. When used as a ligand, TMEDA enhances the reactivity of metal catalysts, leading to improved selectivity and efficiency in processes such as cross-coupling reactions, hydroamination, and polymerization reactions.Additionally, TMEDA can act as a coordinating agent in various organometallic transformations, promoting the formation of reactive intermediates and accelerating reaction rates. Its ability to stabilize and activate metal species makes it a crucial component in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Overall, the application of N1,N1,3-Trimethylbenzene-1,4-diamine in chemical synthesis plays a pivotal role in enabling diverse synthetic transformations and advancing the field of catalysis.