Cas no 63650-24-8 (2-(4-chlorophenoxy)propan-1-ol)

2-(4-Chlorophenoxy)propan-1-ol is a chlorinated aromatic alcohol with the molecular formula C9H11ClO2. This compound features a propanol backbone substituted with a 4-chlorophenoxy group, making it a versatile intermediate in organic synthesis. Its reactive hydroxyl group allows for further functionalization, while the chlorophenoxy moiety contributes to its stability and potential applications in agrochemical and pharmaceutical research. The compound exhibits moderate solubility in organic solvents, facilitating its use in various reaction conditions. Its well-defined structure and purity make it suitable for precise synthetic applications, including the development of specialized fine chemicals and active pharmaceutical ingredients (APIs).
2-(4-chlorophenoxy)propan-1-ol structure
63650-24-8 structure
Product Name:2-(4-chlorophenoxy)propan-1-ol
CAS No:63650-24-8
MF:C9H11ClO2
MW:186.635442018509
MDL:MFCD16302593
CID:1655185
PubChem ID:13259417
Update Time:2025-11-02

2-(4-chlorophenoxy)propan-1-ol Chemical and Physical Properties

Names and Identifiers

    • 2-(4-chlorophenoxy)propan-1-ol
    • 1-propanol, 2-(4-chlorophenoxy)-
    • LogP
    • SCHEMBL1838537
    • DTXSID90532608
    • 2-(p-chlorophenoxy)-1-propanol
    • 63650-24-8
    • EN300-296349
    • 2-(4-chlorophenoxy)-1-propanol
    • 2-(4-chlorophenoxy)-propanol
    • ULXGJWWZHKJAMQ-UHFFFAOYSA-N
    • MDL: MFCD16302593
    • Inchi: 1S/C9H11ClO2/c1-7(6-11)12-9-4-2-8(10)3-5-9/h2-5,7,11H,6H2,1H3
    • InChI Key: ULXGJWWZHKJAMQ-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=CC=1)OC(C)CO

Computed Properties

  • Exact Mass: 186.04483
  • Monoisotopic Mass: 186.0447573g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 122
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.3
  • Topological Polar Surface Area: 29.5?2

Experimental Properties

  • Density: 1.194
  • Boiling Point: 286.4°C at 760 mmHg
  • Flash Point: 127°C
  • Refractive Index: 1.534
  • PSA: 29.46

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Additional information on 2-(4-chlorophenoxy)propan-1-ol

Comprehensive Guide to 2-(4-Chlorophenoxy)propan-1-ol (CAS No. 63650-24-8): Properties, Applications, and Market Insights

2-(4-Chlorophenoxy)propan-1-ol (CAS No. 63650-24-8) is an organic compound widely used in various industrial and research applications. This chlorophenoxy derivative is known for its unique chemical properties, making it valuable in sectors such as pharmaceuticals, agrochemicals, and specialty chemicals. In this article, we delve into the molecular structure, synthesis, applications, and current market trends of this compound, addressing common queries and industry demands.

The molecular formula of 2-(4-Chlorophenoxy)propan-1-ol is C9H11ClO2, featuring a chlorophenoxy group attached to a propanol backbone. Its moderate polarity and solubility in organic solvents make it a versatile intermediate in chemical synthesis. Researchers often explore its role in herbicide formulations and pharmaceutical precursors, aligning with the growing demand for eco-friendly agrochemicals and bioactive molecules.

One of the trending topics in the chemical industry is the shift toward sustainable synthesis methods. 2-(4-Chlorophenoxy)propan-1-ol is frequently discussed in this context due to its potential as a green chemistry intermediate. Recent studies highlight its use in catalytic processes that minimize waste, addressing environmental concerns. This aligns with the increasing number of searches for "eco-friendly chemical intermediates" and "green synthesis of chlorophenoxy compounds" on academic and industrial platforms.

In the pharmaceutical sector, 2-(4-Chlorophenoxy)propan-1-ol serves as a building block for drug development. Its structural motif is found in compounds with potential anti-inflammatory and antimicrobial properties, sparking interest in medicinal chemistry. Online searches often include queries like "applications of chlorophenoxy alcohols in medicine", reflecting its relevance in drug discovery pipelines.

The agrochemical industry leverages 2-(4-Chlorophenoxy)propan-1-ol for formulating selective herbicides. With the global push for precision agriculture, this compound's role in crop protection solutions is gaining traction. Farmers and researchers frequently search for "chlorophenoxy-based herbicides" and "mode of action of phenoxy alcohols", underscoring its practical significance.

From a commercial perspective, the demand for 2-(4-Chlorophenoxy)propan-1-ol is influenced by regional regulations and agricultural trends. Suppliers and manufacturers monitor keywords like "CAS 63650-24-8 suppliers" and "high-purity chlorophenoxy alcohols" to align with buyer needs. Quality standards, such as HPLC purity and residual solvent levels, are critical discussion points in procurement circles.

Safety and handling of 2-(4-Chlorophenoxy)propan-1-ol are also frequently searched topics. While not classified as hazardous under standard protocols, proper storage conditions (e.g., away from strong oxidizers) and personal protective equipment (PPE) recommendations are essential for laboratory and industrial users. These practical aspects are often highlighted in safety data sheets (SDS) and operational guidelines.

In summary, 2-(4-Chlorophenoxy)propan-1-ol (CAS No. 63650-24-8) is a multifaceted compound with expanding applications in green chemistry, pharmaceuticals, and agrochemicals. Its alignment with sustainability goals and precision agriculture trends ensures continued relevance in research and industry. For those seeking detailed technical data or procurement options, focusing on keywords like "chlorophenoxy propanol synthesis" or "63650-24-8 specifications" will yield targeted insights.

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