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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-[2-(methylamino)ethyl]-

CNCCN(CCNC)C Request for Quotation
Chemical Name: 1,2-Ethanediamine, N,N'-dimethyl-N-[2-(methylamino)ethyl]-
CAS Number: 105-84-0
Product Number: AG003DLW(AGN-PC-0JL7HR)
Synonyms:
MDL No:
Molecular Formula: C7H19N3
Molecular Weight: 145.2459

Identification/Properties

Properties
BP:
190.3±8.0°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Refractive Index:
1.4500 to 1.4540
Computed Properties
Molecular Weight:
145.25g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
145.158g/mol
Monoisotopic Mass:
145.158g/mol
Topological Polar Surface Area:
27.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
57.9
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N1,N2-Dimethyl-N1-(2-(methylamino)ethyl)ethane-1,2-diamine, commonly known as $name$, serves as a valuable reagent in chemical synthesis due to its unique properties. In organic chemistry, $name$ is often utilized as a versatile building block in the formation of complex molecules. Its ability to act as a chelating ligand enhances the coordination of metal ions in various catalytic reactions, facilitating the formation of stable intermediates. Additionally, $name$ can participate in reductive amination reactions, playing a crucial role in the synthesis of amines and amine derivatives. Its selective and efficient reactivity makes it an essential component in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.