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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)-

2-Naphthalenecarboxamide, N-(2-ethylphenyl)-3-hydroxy-

CCc1ccccc1NC(=O)c1cc2ccccc2cc1O Request for Quotation
Chemical Name: 2-Naphthalenecarboxamide, N-(2-ethylphenyl)-3-hydroxy-
CAS Number: 68911-98-8
Product Number: AG003S9C(AGN-PC-0JLI2X)
Synonyms:
MDL No:
Molecular Formula: C19H17NO2
Molecular Weight: 291.34378

Identification/Properties

Properties
Storage:
Room Temperature;Keep in dry area;
Computed Properties
Molecular Weight:
291.35g/mol
XLogP3:
5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
291.126g/mol
Monoisotopic Mass:
291.126g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
384
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


N-(2-Ethylphenyl)-3-hydroxy-2-naphthamide is a versatile compound used in chemical synthesis for its unique properties and reactivity. As a key building block in organic chemistry, this compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. With its distinctive structure, N-(2-Ethylphenyl)-3-hydroxy-2-naphthamide enables the formation of complex molecular structures through a range of synthetic transformations, including acylation, condensation, and substitution reactions. Its strategic placement of functional groups facilitates specific interactions and bond formations, making it an indispensable tool for the creation of novel compounds with desirable properties. In the realm of chemical synthesis, N-(2-Ethylphenyl)-3-hydroxy-2-naphthamide plays a crucial role in advancing scientific research and innovation by enabling the efficient and precise construction of molecular architectures for diverse applications.