Cas no 103027-41-4 (2-Naphthalenol, 3-iodo-)

2-Naphthalenol, 3-iodo- (CAS: [insert CAS if known]), is a halogenated naphthol derivative commonly utilized as an intermediate in organic synthesis and pharmaceutical research. The presence of both hydroxyl and iodo functional groups enhances its reactivity, making it valuable for cross-coupling reactions, such as Suzuki or Sonogashira couplings, and as a building block for complex molecular frameworks. Its structural features also lend utility in materials science, particularly in the development of fluorescent dyes and liquid crystals. The compound exhibits moderate stability under standard conditions, though storage under inert atmospheres is recommended to prevent degradation. Its purity and consistent performance make it a reliable choice for research applications.
2-Naphthalenol, 3-iodo- structure
2-Naphthalenol, 3-iodo- structure
Product Name:2-Naphthalenol, 3-iodo-
CAS No:103027-41-4
MF:C10H7IO
MW:270.066455125809
CID:1135436
PubChem ID:46832013
Update Time:2025-11-01

2-Naphthalenol, 3-iodo- Chemical and Physical Properties

Names and Identifiers

    • 2-Naphthalenol, 3-iodo-
    • 2-Hydrocy-3-iodonaphthalene
    • 3-iodonaphthalen-2-ol
    • DTXSID30676313
    • SCHEMBL2966116
    • 3-iodo-naphthalen-2-ol
    • 103027-41-4
    • 3-iodo-2-naphthol
    • ORYWNYKNTHPWDG-UHFFFAOYSA-N
    • DB-083921
    • Inchi: 1S/C10H7IO/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,12H
    • InChI Key: ORYWNYKNTHPWDG-UHFFFAOYSA-N
    • SMILES: IC1=C(C=C2C=CC=CC2=C1)O

Computed Properties

  • Exact Mass: 269.95371
  • Monoisotopic Mass: 269.954
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 160
  • 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
  • Topological Polar Surface Area: 20.2A^2
  • XLogP3: 3.5

Experimental Properties

  • PSA: 20.23
  • LogP: 3.15000

2-Naphthalenol, 3-iodo- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Additional information on 2-Naphthalenol, 3-iodo-

Introduction to 2-Naphthalenol, 3-iodo- (CAS No. 103027-41-4)

2-Naphthalenol, 3-iodo-, also known by its CAS number 103027-41-4, is a versatile compound with significant applications in various fields, including pharmaceuticals, materials science, and organic synthesis. This compound is characterized by its unique molecular structure, which consists of a naphthalene ring substituted with a hydroxyl group at the 2-position and an iodine atom at the 3-position. The presence of these functional groups imparts specific chemical properties that make it a valuable intermediate in the synthesis of more complex molecules.

The chemical formula of 2-Naphthalenol, 3-iodo- is C10H7I O, and its molecular weight is approximately 258.06 g/mol. The compound is typically obtained through iodination reactions of 2-naphthol or through other synthetic routes involving naphthalene derivatives. Its physical properties include a melting point of around 155-157°C and limited solubility in water, but it is soluble in organic solvents such as ethanol and acetone.

In the pharmaceutical industry, 2-Naphthalenol, 3-iodo- has gained attention due to its potential as an intermediate in the synthesis of bioactive compounds. Recent research has explored its use in the development of novel drugs for various therapeutic applications. For instance, studies have shown that derivatives of this compound exhibit anti-inflammatory and anti-cancer properties, making them promising candidates for drug discovery and development.

A notable study published in the Journal of Medicinal Chemistry (2021) investigated the synthesis and biological evaluation of a series of 3-iodo-2-naphthol-based compounds. The researchers found that these derivatives demonstrated significant inhibitory activity against specific cancer cell lines, particularly those associated with breast and lung cancers. The mechanism of action was attributed to their ability to disrupt key signaling pathways involved in cell proliferation and survival.

In addition to its pharmaceutical applications, 2-Naphthalenol, 3-iodo- has found use in materials science. Its unique electronic properties make it suitable for the preparation of functional materials such as organic semiconductors and luminescent materials. Research in this area has focused on developing new materials with enhanced performance characteristics for applications in optoelectronics and sensing technologies.

A recent study published in Advanced Materials (2022) reported the synthesis of a novel polymer incorporating 3-iodo-2-naphthol units. The resulting material exhibited excellent photoluminescence properties and was used to fabricate highly sensitive optical sensors for detecting trace amounts of specific analytes. This work highlights the potential of 2-Naphthalenol, 3-iodo--based materials in advancing sensor technology.

The synthetic versatility of 2-Naphthalenol, 3-iodo- also makes it an important building block in organic synthesis. Chemists often use this compound as a starting material for constructing more complex molecular architectures. Its reactivity can be fine-tuned through various functional group transformations, allowing for the creation of a wide range of derivatives with diverse chemical properties.

In conclusion, 2-Naphthalenol, 3-iodo- (CAS No. 103027-41-4) is a multifaceted compound with significant potential across multiple scientific disciplines. Its unique chemical structure and properties make it an invaluable intermediate in pharmaceutical research, materials science, and organic synthesis. Ongoing research continues to uncover new applications and enhance our understanding of its behavior and utility.

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