Cas no 121629-21-8 (4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid)

4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid is a biphenyl derivative featuring both a carboxylic acid and a hydroxyl functional group, making it a versatile intermediate in organic synthesis and pharmaceutical applications. The compound's distinct structure allows for selective reactivity, enabling its use in the preparation of fine chemicals, ligands, and bioactive molecules. Its hydroxyl and carboxyl groups provide sites for further functionalization, such as esterification or etherification, enhancing its utility in material science and medicinal chemistry. The biphenyl core contributes to stability and rigidity, beneficial for designing compounds with specific steric and electronic properties. This product is suitable for research and industrial applications requiring precise molecular modifications.
4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid structure
121629-21-8 structure
Product Name:4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid
CAS No:121629-21-8
MF:C13H10O3
MW:214.216703891754
MDL:MFCD01910126
CID:104683
PubChem ID:722432
Update Time:2025-05-24

4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid
    • [1,1'-Biphenyl]-3-carboxylicacid, 4'-hydroxy-
    • 3-(4-HYDROXYPHENYL)BENZOIC ACID
    • 4-HYDROXYBIPHENYL-3-CARBOXYLIC ACID
    • 3'-carboxybiphenyl-4-ol
    • 4'-hydroxy[1,1'-biphenyl]-3-carboxylic acid
    • 4'-hydroxy-1,1'-biphenyl-3-carboxylic acid
    • 4'-Hydroxy-biphenyl-3-carbonsaeure
    • 4'-Hydroxybiphenyl-3-carboxylic acid
    • 4'-Hydroxy-biphenyl-3-carboxylic acid
    • AC1LF3K0
    • ACMC-1CANT
    • IFLab1_004221
    • IFLab2_000269
    • Oprea1_229211
    • SureCN1165306
    • 4'-hydroxybiphenyl-3-carboxylic acid(SALTDATA: FREE)
    • BS-21032
    • 4'-hydroxy biphenyl-3-carboxylic acid
    • Z56887634
    • JSX
    • F0875-0028
    • 121629-21-8
    • CHEMBL4093894
    • WEA62921
    • 4'-Hydroxy-3-biphenylcarboxylic acid
    • SR-01000446515
    • SCHEMBL1165306
    • MFCD01910126
    • WINNQOZTIDYENK-UHFFFAOYSA-N
    • 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylicacid
    • EU-0039746
    • BB 0223345
    • F79735
    • IDI1_019295
    • SR-01000446515-1
    • [1,1'-Biphenyl]-3-carboxylic acid, 4'-hydroxy-
    • AKOS001065181
    • EN300-04179
    • DTXSID00352293
    • HMS1423P19
    • 4'-Hydroxy[1,1'-biphenyl]-3-carboxylic Acid; 3-(4-Hydroxyphenyl)benzoic Acid;
    • DB-349366
    • MDL: MFCD01910126
    • Inchi: 1S/C13H10O3/c14-12-6-4-9(5-7-12)10-2-1-3-11(8-10)13(15)16/h1-8,14H,(H,15,16)
    • InChI Key: WINNQOZTIDYENK-UHFFFAOYSA-N
    • SMILES: OC1C=CC(=CC=1)C1C=CC=C(C(=O)O)C=1

Computed Properties

  • Exact Mass: 214.063
  • Monoisotopic Mass: 214.062994177g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 2
  • Complexity: 244
  • 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: 3.3
  • Topological Polar Surface Area: 57.5?2

Experimental Properties

  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 441.0±28.0 °C at 760 mmHg
  • Flash Point: 234.6±20.5 °C
  • PSA: 57.53
  • Vapor Pressure: 0.0±1.1 mmHg at 25°C

4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid Security Information

4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid Pricemore >>

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Additional information on 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid

Recent Advances in the Study of 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid (CAS: 121629-21-8)

The compound 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid (CAS: 121629-21-8) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This biphenyl derivative, characterized by its hydroxyl and carboxylic acid functional groups, has shown promising potential in various therapeutic applications, including anti-inflammatory, anticancer, and antimicrobial activities. Recent studies have focused on elucidating its molecular mechanisms, optimizing its synthesis, and exploring its pharmacological properties.

One of the key areas of investigation has been the compound's role as a building block for more complex molecules. Researchers have utilized 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid as a precursor in the synthesis of novel drug candidates. Its unique structural features allow for facile modification, enabling the development of derivatives with enhanced bioactivity and selectivity. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated the compound's utility in designing inhibitors targeting specific enzymes involved in inflammatory pathways.

In addition to its synthetic applications, recent research has explored the compound's direct biological effects. A study conducted by a team at the University of Cambridge revealed that 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid exhibits potent antioxidant properties, scavenging free radicals and reducing oxidative stress in cellular models. These findings suggest its potential as a therapeutic agent for diseases associated with oxidative damage, such as neurodegenerative disorders and cardiovascular diseases.

Another significant advancement involves the optimization of the compound's pharmacokinetic properties. Researchers have employed advanced computational modeling and structure-activity relationship (SAR) studies to improve its bioavailability and metabolic stability. A recent publication in Bioorganic & Medicinal Chemistry Letters highlighted the successful modification of the compound's scaffold to enhance its absorption and distribution profiles, paving the way for its development as a viable drug candidate.

Despite these promising developments, challenges remain in the clinical translation of 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid. Issues such as solubility, toxicity, and off-target effects need to be addressed through further research. However, the compound's versatility and demonstrated bioactivity make it a valuable focus for ongoing studies in the chemical biology and pharmaceutical fields.

In conclusion, 4'-Hydroxy-[1,1'-biphenyl]-3-carboxylic acid (CAS: 121629-21-8) represents a compelling area of research with significant therapeutic potential. Recent studies have expanded our understanding of its molecular mechanisms, synthetic utility, and pharmacological effects, laying the groundwork for future drug development efforts. Continued exploration of this compound and its derivatives is expected to yield innovative solutions for a range of medical challenges.

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