Cas no 125110-82-9 (4,4-difluoropentanoic acid)

4,4-difluoropentanoic acid structure
4,4-difluoropentanoic acid structure
Product Name:4,4-difluoropentanoic acid
CAS No:125110-82-9
MF:C5H8F2O2
MW:138.112628936768
CID:2101579
Update Time:2025-07-20

4,4-difluoropentanoic acid Chemical and Physical Properties

Names and Identifiers

    • 4,4-difluoropentanoic acid
    • Inchi: 1S/C5H8F2O2/c1-5(6,7)3-2-4(8)9/h2-3H2,1H3,(H,8,9)
    • InChI Key: IMDBVJNJIGOFTM-UHFFFAOYSA-N
    • SMILES: FC(C)(CCC(=O)O)F

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 3

4,4-difluoropentanoic acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
D268215-5mg
4,4-Difluorpentanoic acid
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$ 140.00 2022-06-05
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$ 235.00 2022-06-05
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NAN JING YAO SHI KE JI GU FEN Co., Ltd.
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NAN JING YAO SHI KE JI GU FEN Co., Ltd.
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abcr
AB402642-250mg
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abcr
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Ambeed
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Additional information on 4,4-difluoropentanoic acid

Recent Advances in the Application of 4,4-Difluoropentanoic Acid (CAS: 125110-82-9) in Chemical Biology and Pharmaceutical Research

4,4-Difluoropentanoic acid (CAS: 125110-82-9) has emerged as a key intermediate in the synthesis of bioactive molecules and pharmaceutical agents. Recent studies have highlighted its utility in the development of novel therapeutics, particularly in the areas of enzyme inhibition and prodrug design. This research briefing provides an overview of the latest advancements involving this compound, focusing on its chemical properties, synthetic applications, and biological activities.

A study published in the Journal of Medicinal Chemistry (2023) demonstrated the use of 4,4-difluoropentanoic acid as a building block for the synthesis of potent histone deacetylase (HDAC) inhibitors. The researchers utilized the compound's unique fluorination pattern to enhance the metabolic stability and binding affinity of their inhibitors, resulting in improved pharmacokinetic profiles. This work underscores the growing importance of fluorinated compounds in drug design.

In the field of prodrug development, a recent patent application (WO2023051234) describes novel ester derivatives of 4,4-difluoropentanoic acid designed to improve the oral bioavailability of challenging drug candidates. The fluorinated moiety was found to significantly enhance membrane permeability while maintaining favorable toxicity profiles. These findings suggest promising applications for this compound in overcoming formulation challenges for poorly soluble active pharmaceutical ingredients.

Analytical chemistry advancements have also been reported for 125110-82-9. A 2024 study in Analytical and Bioanalytical Chemistry presented a novel LC-MS/MS method for the sensitive detection and quantification of 4,4-difluoropentanoic acid and its metabolites in biological matrices. This method achieved detection limits below 1 ng/mL, enabling more accurate pharmacokinetic studies of compounds derived from this intermediate.

The compound's mechanism of action has been further elucidated through recent structural biology studies. Cryo-EM analysis published in Nature Structural & Molecular Biology (2024) revealed how 4,4-difluoropentanoic acid-containing inhibitors interact with their protein targets at atomic resolution. These structural insights are guiding the rational design of next-generation therapeutics with improved selectivity and potency.

Looking forward, research directions for 4,4-difluoropentanoic acid appear to be expanding into new therapeutic areas. Preliminary data presented at the 2024 American Chemical Society National Meeting suggests potential applications in targeted protein degradation and PROTAC development. The compound's versatility as both a linker and functional moiety makes it particularly valuable in these emerging drug discovery paradigms.

In conclusion, 4,4-difluoropentanoic acid (125110-82-9) continues to demonstrate significant value in pharmaceutical research and development. Its applications span from traditional small molecule drug design to cutting-edge therapeutic modalities, supported by ongoing advances in synthetic chemistry, structural biology, and analytical methodology. Future research will likely uncover additional utilities for this versatile compound as chemical biology tools become increasingly sophisticated.

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