Cas no 50823-88-6 (4-(chlorodifluoromethoxy)phenylmethanol)

4-(Chlorodifluoromethoxy)phenylmethanol is a versatile fluorinated aromatic alcohol with applications in pharmaceutical and agrochemical synthesis. Its key structural features include a chlorodifluoromethoxy group, which enhances lipophilicity and metabolic stability, and a hydroxymethyl moiety that serves as a reactive handle for further derivatization. The compound is particularly valuable in the development of bioactive molecules due to its ability to modulate electronic and steric properties. Its stability under various reaction conditions makes it a reliable intermediate for constructing complex molecular architectures. The presence of both fluorine and chlorine atoms contributes to its utility in designing compounds with tailored physicochemical properties.
4-(chlorodifluoromethoxy)phenylmethanol structure
50823-88-6 structure
Product Name:4-(chlorodifluoromethoxy)phenylmethanol
CAS No:50823-88-6
MF:C8H7ClF2O2
MW:208.589788675308
CID:1569679
PubChem ID:45156944
Update Time:2025-06-11

4-(chlorodifluoromethoxy)phenylmethanol Chemical and Physical Properties

Names and Identifiers

    • [4-[chloro(difluoro)methoxy]phenyl]methanol
    • 4-(Chlorodifluoromethoxy)benzyl alcohol
    • CTK4J3209
    • MolPort-004-962-119
    • PC5470
    • SBB094098
    • AG-F-71245
    • [4-(chlorodifluoromethoxy)phenyl]methanol
    • KB-85784
    • (4-[CHLORO(DIFLUORO)METHOXY]PHENYL)METHANOL
    • DTXSID70669527
    • 50823-88-6
    • {4-[Chloro(difluoro)methoxy]phenyl}methanol
    • HFUMPXYULWQMCI-UHFFFAOYSA-N
    • MFCD11052962
    • CS-0237289
    • 4-(Chlorodifluoromethoxxy)benzyl alcohol
    • EN300-181595
    • AKOS025395474
    • 4-(chlorodifluoromethoxy)phenylmethanol
    • Inchi: 1S/C8H7ClF2O2/c9-8(10,11)13-7-3-1-6(5-12)2-4-7/h1-4,12H,5H2
    • InChI Key: HFUMPXYULWQMCI-UHFFFAOYSA-N
    • SMILES: ClC(OC1C=CC(CO)=CC=1)(F)F

Computed Properties

  • Exact Mass: 208.01031
  • Monoisotopic Mass: 208.0102635g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 158
  • 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: 2.6
  • Topological Polar Surface Area: 29.5?2

Experimental Properties

  • PSA: 29.46

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4-(chlorodifluoromethoxy)phenylmethanol Suppliers

Amadis Chemical Company Limited
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(CAS:50823-88-6)4-(chlorodifluoromethoxy)phenylmethanol
Order Number:A1235577
Stock Status:in Stock
Quantity:250mg
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 19:18
Price ($):1696

Additional information on 4-(chlorodifluoromethoxy)phenylmethanol

Research Briefing on 4-(chlorodifluoromethoxy)phenylmethanol (CAS: 50823-88-6): Recent Advances and Applications

4-(chlorodifluoromethoxy)phenylmethanol (CAS: 50823-88-6) is a fluorinated aromatic alcohol that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential applications in drug development. This compound, characterized by the presence of a chlorodifluoromethoxy group and a phenylmethanol moiety, serves as a versatile intermediate in the synthesis of various bioactive molecules. Recent studies have explored its utility in the design of novel therapeutic agents, particularly in the context of anti-inflammatory, antimicrobial, and anticancer applications.

One of the most notable advancements in the research of 4-(chlorodifluoromethoxy)phenylmethanol is its role as a key intermediate in the synthesis of fluorinated analogs of biologically active compounds. Fluorination is a common strategy in medicinal chemistry to enhance the metabolic stability, bioavailability, and binding affinity of drug candidates. The chlorodifluoromethoxy group in this compound provides a unique handle for further chemical modifications, enabling the development of derivatives with tailored pharmacological properties. Recent publications have highlighted its use in the synthesis of fluorinated tyrosine kinase inhibitors and G-protein-coupled receptor (GPCR) modulators, which are of great interest in targeted cancer therapies and neurological disorders.

In addition to its synthetic utility, 4-(chlorodifluoromethoxy)phenylmethanol has been investigated for its direct biological activities. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit potent inhibitory effects against cyclooxygenase-2 (COX-2), an enzyme implicated in inflammatory processes. The study reported that the introduction of the chlorodifluoromethoxy group significantly enhanced the selectivity and potency of the inhibitors compared to their non-fluorinated counterparts. These findings underscore the potential of 4-(chlorodifluoromethoxy)phenylmethanol as a scaffold for developing next-generation anti-inflammatory drugs.

Another area of active research involves the antimicrobial properties of 4-(chlorodifluoromethoxy)phenylmethanol derivatives. A recent preprint on bioRxiv detailed the synthesis and evaluation of a series of fluorinated phenylmethanol derivatives against multidrug-resistant bacterial strains. The results indicated that the chlorodifluoromethoxy moiety contributed to improved membrane permeability and target engagement, leading to enhanced antibacterial activity. These insights are particularly relevant in the context of the growing global threat of antibiotic resistance, as they provide a foundation for designing new antimicrobial agents with novel mechanisms of action.

Despite these promising developments, challenges remain in the optimization and clinical translation of 4-(chlorodifluoromethoxy)phenylmethanol-based compounds. Issues such as metabolic stability, toxicity profiles, and scalable synthesis need to be addressed to fully realize their therapeutic potential. Ongoing research efforts are focused on leveraging advanced computational modeling and high-throughput screening to identify optimal derivatives with favorable pharmacokinetic and safety profiles. Collaborative initiatives between academic institutions and pharmaceutical companies are also underway to accelerate the development of these compounds into viable drug candidates.

In conclusion, 4-(chlorodifluoromethoxy)phenylmethanol (CAS: 50823-88-6) represents a promising scaffold in medicinal chemistry, with demonstrated applications in anti-inflammatory, antimicrobial, and anticancer drug discovery. Recent studies have shed light on its synthetic versatility and biological activities, paving the way for future innovations. As research in this area continues to evolve, it is anticipated that this compound and its derivatives will play an increasingly important role in addressing unmet medical needs and advancing the field of chemical biology.

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Amadis Chemical Company Limited
(CAS:50823-88-6)4-(chlorodifluoromethoxy)phenylmethanol
A1235577
Purity:99%
Quantity:250mg
Price ($):1696
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