Cas no 40492-93-1 (7-chloronaphthalen-2-ol)

7-chloronaphthalen-2-ol structure
7-chloronaphthalen-2-ol structure
Product Name:7-chloronaphthalen-2-ol
CAS No:40492-93-1
MF:C10H7ClO
MW:178.614981889725
CID:925830
PubChem ID:97289
Update Time:2025-04-23

7-chloronaphthalen-2-ol Chemical and Physical Properties

Names and Identifiers

    • 7-chloronaphthalen-2-ol
    • 2-Chloro-7-hydroxynaphthalene
    • 2-Naphthalenol, 7-chloro-
    • 7-Chlor-[2]naphthol
    • 7-Chlor-2-hydroxy-naphthalin
    • 7-Chlor-2-naphthol
    • 7-Chlor-naphthol-(2)
    • 7-chloro-[2]naphthol
    • 7-chloro-2-naphthalenol
    • 7-Chloro-2-naphthol
    • AC1L3Y7F
    • AC1Q3RL1
    • NSC112383
    • SureCN6689974
    • P7OU33U1IX
    • QSDSWPOSISCSSI-UHFFFAOYSA-N
    • CS-0173237
    • SMR001573846
    • ZB1010
    • NSC-112383
    • BS-50160
    • MLS002706440
    • SCHEMBL6689974
    • FT-0750458
    • DTXSID80193505
    • 40492-93-1
    • N14581
    • NSC 112383
    • UNII-P7OU33U1IX
    • CHEMBL1865678
    • 2-Chloro-7-naphthol
    • MFCD17012291
    • DTXCID50115996
    • SY027174
    • DB-083692
    • Inchi: 1S/C10H7ClO/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h1-6,12H
    • InChI Key: QSDSWPOSISCSSI-UHFFFAOYSA-N
    • SMILES: ClC1C=CC2=CC=C(C=C2C=1)O

Computed Properties

  • Exact Mass: 178.01861
  • Monoisotopic Mass: 178.0185425g/mol
  • 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
  • XLogP3: 3.8
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • PSA: 20.23
  • LogP: 3.19880

7-chloronaphthalen-2-ol Pricemore >>

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Additional information on 7-chloronaphthalen-2-ol

7-Chloronaphthalen-2-ol: A Comprehensive Overview

7-Chloronaphthalen-2-ol, also known by its CAS number CAS 40492-93-1, is a chemically significant compound that has garnered attention in various fields of research and industry. This compound belongs to the class of naphthol derivatives and is characterized by the presence of a hydroxyl group (-OH) at the 2-position and a chlorine atom at the 7-position of the naphthalene ring system. The structure of 7-chloronaphthalen-2-ol makes it a valuable molecule for exploring its unique chemical properties, reactivity, and potential applications.

The synthesis of 7-chloronaphthalen-2-ol has been extensively studied, with researchers focusing on developing efficient and environmentally friendly methods. Recent advancements in catalytic processes have enabled the selective introduction of the hydroxyl and chlorine groups onto the naphthalene framework. For instance, studies have demonstrated the use of transition metal catalysts to achieve high yields and selectivity in the synthesis of this compound. These methods not only enhance the scalability of production but also align with the growing demand for sustainable chemical manufacturing practices.

In terms of physical properties, 7-chloronaphthalen-2-ol exhibits a melting point of approximately 155°C and is sparingly soluble in water. Its solubility increases significantly in organic solvents such as dichloromethane and ethyl acetate, making it suitable for various organic reactions. The presence of both hydroxyl and chlorine groups imparts unique electronic properties to the molecule, which influence its reactivity in different chemical environments. For example, the hydroxyl group can act as a nucleophile in substitution reactions, while the chlorine atom can serve as an electrophilic site under certain conditions.

The application of 7-chloronaphthalen-2-ol spans across multiple domains, including pharmaceuticals, agrochemicals, and materials science. In the pharmaceutical industry, this compound has been explored as a potential lead molecule for drug development due to its ability to interact with various biological targets. Recent studies have highlighted its role as an inhibitor of certain enzymes involved in metabolic pathways, suggesting its potential as a therapeutic agent.

In agrochemicals, 7-chloronaphthalen-2-ol has been investigated for its pesticidal properties. Research indicates that this compound exhibits moderate activity against several agricultural pests, making it a candidate for further development into eco-friendly pesticides. Additionally, its structural versatility allows for further modification to enhance efficacy and reduce environmental impact.

The environmental impact of 7-chloronaphthalen-2-ol is another area of interest for researchers. Studies have been conducted to assess its biodegradability and toxicity to aquatic organisms. Results suggest that under aerobic conditions, this compound undergoes slow biodegradation, raising concerns about its persistence in natural ecosystems. However, ongoing research aims to develop methods to accelerate its breakdown using microbial consortia or enzymatic treatments.

In conclusion, 7-chloronaphthalen-2-ol (CAS 40492-93) stands out as a versatile compound with significant potential across various industries. Its unique chemical structure, coupled with recent advancements in synthesis and application techniques, positions it as a valuable tool for future innovations. As research continues to uncover new insights into its properties and behavior, this compound is poised to play an increasingly important role in both academic and industrial settings.

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