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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)-

1,2-Ethanediamine, N,N-dimethyl-N'-phenyl-

CN(CCNc1ccccc1)C Request for Quotation
Chemical Name: 1,2-Ethanediamine, N,N-dimethyl-N'-phenyl-
CAS Number: 6711-46-2
Product Number: AG00FUYD(AGN-PC-0JLT3D)
Synonyms:
MDL No:
Molecular Formula: C10H16N2
Molecular Weight: 164.2474

Identification/Properties

Computed Properties
Molecular Weight:
164.252g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
164.131g/mol
Monoisotopic Mass:
164.131g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
106
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N1, N1-Dimethyl-N2-phenyl-1,2-ethanediamine, also known as $name$, is a versatile compound commonly utilized in chemical synthesis. This compound serves as an important building block in the creation of various organic molecules, particularly in the pharmaceutical and agrochemical industries. One of the key applications of $name$ in chemical synthesis is its role as a chelating agent. Its unique molecular structure allows it to form stable complexes with metal ions, which is essential in various catalytic reactions and metal-mediated transformations. By chelating with metal ions, $name$ can facilitate the formation of new bonds, enhance reaction selectivity, and improve overall reaction efficiency.Additionally, $name$ can act as a ligand in coordination chemistry, participating in metal complexation reactions to form coordination compounds. These complexes often exhibit interesting properties and reactivity, making them valuable intermediates in the synthesis of complex organic molecules.Overall, the versatility of N1, N1-Dimethyl-N2-phenyl-1,2-ethanediamine makes it a valuable tool in chemical synthesis, allowing for the construction of diverse organic compounds with potential applications in drug discovery, materials science, and other fields.