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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-Naphthalenecarboxamide, N-(2-aminoethyl)-

NCCNC(=O)c1cccc2c1cccc2 Request for Quotation
Chemical Name: 1-Naphthalenecarboxamide, N-(2-aminoethyl)-
CAS Number: 121494-75-5
Product Number: AG00IKDM(AGN-PC-02MR23)
Synonyms:
MDL No:
Molecular Formula: C13H14N2O
Molecular Weight: 214.2631

Identification/Properties

Computed Properties
Molecular Weight:
214.268g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
214.111g/mol
Monoisotopic Mass:
214.111g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
242
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


1-Naphthalenecarboxamide, N-(2-aminoethyl)- is a versatile compound widely used in chemical synthesis. This compound is commonly employed as a building block in the synthesis of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and functional groups make it suitable for a range of applications in organic chemistry.In chemical synthesis, 1-Naphthalenecarboxamide, N-(2-aminoethyl)- can act as a key intermediate in the production of complex molecules. Its aminoethyl group allows for selective functionalization through various chemical reactions such as acylation, alkylation, and hydrogenation. This compound can participate in peptide coupling reactions, enabling the formation of peptide bonds for the synthesis of peptides and peptidomimetics.Furthermore, 1-Naphthalenecarboxamide, N-(2-aminoethyl)- can be utilized in the construction of heterocyclic compounds, which are essential building blocks in drug discovery and material science. Its aromatic naphthalene ring provides additional versatility and reactivity, allowing for the creation of diverse chemical structures with specific properties.Overall, the application of 1-Naphthalenecarboxamide, N-(2-aminoethyl)- in chemical synthesis offers researchers a valuable tool for designing and synthesizing novel compounds with potential applications in various industries.