Cas no 4711-68-6 (N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide)

N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide is a synthetic organic compound featuring a naphthamide core substituted with a hydroxyl group at the 3-position and an ethoxyphenyl moiety at the amide nitrogen. This structure imparts unique photophysical and coordination properties, making it valuable in applications such as fluorescent dyes, organic semiconductors, and chelating agents. The ethoxy group enhances solubility in organic solvents, while the hydroxyl group provides a reactive site for further functionalization or metal binding. Its stability and tunable electronic characteristics make it suitable for advanced material research and specialized chemical synthesis. The compound is typically characterized by high purity and consistent performance in experimental and industrial settings.
N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide structure
4711-68-6 structure
Product Name:N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide
CAS No:4711-68-6
MF:C19H17NO3
MW:307.343185186386
CID:45254
PubChem ID:78443
Update Time:2025-08-05

N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide Chemical and Physical Properties

Names and Identifiers

    • N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide
    • Azoic Coupling Component 30
    • N-(4-ethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide
    • NAPHTHOL AS-VL
    • 2-Hydroxy-3-naphthoesaeure-p-phenetidid
    • 3-Hydroxy-[2]naphthoesaeure-p-phenetidid
    • 3-hydroxy-[2]naphthoic acid p-phenetidide
    • 3-Hydroxy-2-naphtho-p-phenetidide
    • 4'-ethoxy-3-hydroxy-2-naphthanilide
    • Azoic coupling component 46
    • C.I. Azoic Coupling Component 30
    • C.I. Azoic Coupling Component 46
    • Cibanaphthol RPH
    • NSC50690
    • cid_78443
    • A918683
    • DTXSID5063570
    • EC 225-200-7
    • CI 37559
    • NSC-50690
    • CHEBI:122078
    • SR-01000513141-1
    • Oprea1_239420
    • N-(4-ethoxyphenyl)-3-oxidanyl-naphthalene-2-carboxamide
    • Q27210711
    • 2-Naphtho-p-phenetidide, 3-hydroxy-
    • UNII-ED3VQI55T0
    • CBDivE_012078
    • N-(4-ethoxyphenyl)-3-hydroxy-naphthalene-2-carboxamide
    • Oprea1_874331
    • NSC 50690
    • HMS2886N22
    • SR-01000513141
    • CHEMBL1388703
    • SMR000528245
    • AKOS000592774
    • 1-Hydroxy-3-Naphthoyl-P-Ethoxy Aniline
    • 2-Naphthalenecarboxamide, N-(4-ethoxyphenyl)-3-hydroxy-
    • C.I. 37559
    • 3-hydroxy-N-p-phenetyl-2-naphthamide
    • 2-HYDROXY-3-NAPHTHOYL-P-ETHOXYANILINE
    • BDBM80521
    • NS00007701
    • 4711-68-6
    • CS-0362287
    • ED3VQI55T0
    • DYCOSTHOL AS-VL
    • NCGC00246827-01
    • EINECS 225-200-7
    • N-(4-ethoxyphenyl)-3-hydroxy-2-naphthalenecarboxamide
    • SCHEMBL2743100
    • AG-690/36740014
    • MLS000736677
    • FYJKEJZGNQVNLC-UHFFFAOYSA-N
    • MDL： MFCD00476996
    • Inchi： 1S/C19H17NO3/c1-2-23-16-9-7-15(8-10-16)20-19(22)17-11-13-5-3-4-6-14(13)12-18(17)21/h3-12,21H,2H2,1H3,(H,20,22)
    • InChI Key： FYJKEJZGNQVNLC-UHFFFAOYSA-N
    • SMILES： OC1C=C2C=CC=CC2=CC=1C(NC1C=CC(=CC=1)OCC)=O

Computed Properties

  • Exact Mass: 307.12100
  • Monoisotopic Mass: 307.121
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 5
  • Complexity: 392
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 9
  • XLogP3: 4.5
  • Topological Polar Surface Area: 58.6A^2

Experimental Properties

  • Density: 1.273
  • Melting Point: 217~219℃
  • Boiling Point: 438.7°C at 760 mmHg
  • Flash Point: 219.1 °C
  • Refractive Index: 1.686
  • PSA: 58.56000
  • LogP: 4.26940

N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide Customs Data

  • HS CODE：2924299090
  • Customs Data：

    China Customs Code:

    2924299090

    Overview:

    2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide Suppliers

Tiancheng Chemical (Jiangsu) Co., Ltd
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(CAS:4711-68-6)色酚AS-VL
Order Number:LE26960462
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 13:00
Price ($):discuss personally

N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide Related Literature

Additional information on N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide

Professional Introduction to N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide (CAS No. 4711-68-6)

N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide, identified by its Chemical Abstracts Service number CAS No. 4711-68-6, is a compound of significant interest in the field of chemical and pharmaceutical research. This molecule, featuring a naphthamide core structure, has garnered attention due to its potential biological activities and structural properties that make it a valuable candidate for further investigation in drug discovery and therapeutic development.

The naphthamide moiety is a key structural feature of this compound, contributing to its unique chemical and biological properties. Naphthamides are known for their broad spectrum of biological activities, including antimicrobial, anti-inflammatory, and anticancer effects. The presence of both hydroxyl and ethoxy substituents in the structure of N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide enhances its potential as a pharmacophore, allowing for selective interactions with biological targets.

In recent years, there has been a growing interest in developing novel therapeutic agents based on naphthamide derivatives. These compounds have shown promise in preclinical studies, particularly in the treatment of various diseases. The hydroxyl group in the molecule can participate in hydrogen bonding interactions, which is crucial for binding to biological targets with high affinity. Additionally, the ethoxy group can influence the electronic properties of the molecule, affecting its reactivity and biological activity.

One of the most compelling aspects of N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide is its potential application in oncology research. Naphthamides have been investigated as inhibitors of proteasome activity, which is essential for cancer cell survival. The structural features of this compound may allow it to interact with specific proteasome subunits, leading to the development of new anticancer drugs. Furthermore, its ability to modulate other cellular pathways involved in cancer progression makes it a promising candidate for further exploration.

The synthesis of N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide

The pharmacological profile of N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide

In vitro studies have also revealed that N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide

The development of novel drug candidates often involves structural modifications to optimize pharmacokinetic properties such as solubility, bioavailability, and metabolic stability. In the case of N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide

The future prospects for N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide

In conclusion, N-(4-Ethoxyphenyl)-3-hydroxy-2-naphthamide (CAS No. 4711-68-6)

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Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:4711-68-6)色酚AS-VL
LE26960462
Purity:99%
Quantity:25KG,200KG,1000KG
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