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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)-

Ethanediamide, N-(2-ethoxyphenyl)-N'-(2-ethylphenyl)-

CCOc1ccccc1NC(=O)C(=O)Nc1ccccc1CC Request for Quotation
Chemical Name: Ethanediamide, N-(2-ethoxyphenyl)-N'-(2-ethylphenyl)-
CAS Number: 23949-66-8
Product Number: AG0039VC(AGN-PC-0JLYKC)
Synonyms:
MDL No:
Molecular Formula: C18H20N2O3
Molecular Weight: 312.3630

Identification/Properties

Computed Properties
Molecular Weight:
312.369g/mol
XLogP3:
3.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
312.147g/mol
Monoisotopic Mass:
312.147g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
400
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-(2-Ethoxyphenyl)-N2-(2-ethylphenyl)ethanediamide, referred to as $name$, is a versatile compound commonly utilized in chemical synthesis. This compound serves as a key building block in organic chemistry, specifically in the development of novel pharmaceuticals and agrochemicals. Its unique structure provides opportunities for creating various derivatives with tailored functionalities, making it a valuable tool for medicinal and agricultural research. In chemical synthesis, $name$ is often employed as a coupling agent or intermediate in the formation of complex molecules, offering a strategic approach to designing new compounds with enhanced biological activities. Furthermore, the presence of both ethoxy and ethylphenyl groups in the molecule imparts specific reactivity profiles that can be harnessed to achieve precise transformations and structural modifications. The application of N1-(2-Ethoxyphenyl)-N2-(2-ethylphenyl)ethanediamide in chemical synthesis underscores its importance in advancing the frontier of organic chemistry and driving innovation in the development of next-generation materials and bioactive compounds.