Cas no 141244-86-2 (2-(2,4-Dibromophenoxy)acetohydrazide)

2-(2,4-Dibromophenoxy)acetohydrazide is a brominated aromatic hydrazide compound with applications in organic synthesis and pharmaceutical research. Its distinct structure, featuring a dibromophenoxy moiety linked to an acetohydrazide group, makes it a valuable intermediate for the development of specialized chemical derivatives. The presence of bromine atoms enhances its reactivity in substitution and coupling reactions, while the hydrazide functionality allows for further derivatization, such as the formation of heterocyclic compounds. This compound is particularly useful in medicinal chemistry for designing bioactive molecules due to its potential as a scaffold for pharmacophores. It is typically handled under controlled conditions due to its sensitivity to moisture and light.
2-(2,4-Dibromophenoxy)acetohydrazide structure
141244-86-2 structure
Product Name:2-(2,4-Dibromophenoxy)acetohydrazide
CAS No:141244-86-2
MF:C8H8Br2N2O2
MW:323.969320297241
MDL:MFCD00098698
CID:1077409
PubChem ID:358746
Update Time:2025-11-02

2-(2,4-Dibromophenoxy)acetohydrazide Chemical and Physical Properties

Names and Identifiers

    • 2-(2,4-Dibromophenoxy)acetohydrazide
    • ALBB-002750
    • SR-01000636450-1
    • MFCD00098698
    • 141244-86-2
    • NSC-618810
    • AB00083127-01
    • DTXSID20326855
    • VS-04255
    • CS-0316483
    • STK036070
    • NSC618810
    • SB86082
    • BBL014288
    • CCG-46776
    • AKOS000305737
    • (2,4-DIBROMO-PHENOXY)-ACETIC ACID HYDRAZIDE
    • MDL: MFCD00098698
    • Inchi: 1S/C8H8Br2N2O2/c9-5-1-2-7(6(10)3-5)14-4-8(13)12-11/h1-3H,4,11H2,(H,12,13)
    • InChI Key: ZLCWJMAWCQNODX-UHFFFAOYSA-N
    • SMILES: BrC1C=C(C=CC=1OCC(NN)=O)Br

Computed Properties

  • Exact Mass: 323.89320g/mol
  • Monoisotopic Mass: 321.89525g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 204
  • 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: 1.9
  • Topological Polar Surface Area: 64.4?2

Experimental Properties

  • Density: 1.9±0.1 g/cm3
  • Boiling Point: 481.3±35.0 °C at 760 mmHg
  • Flash Point: 244.9±25.9 °C
  • Vapor Pressure: 0.0±1.2 mmHg at 25°C

2-(2,4-Dibromophenoxy)acetohydrazide Security Information

2-(2,4-Dibromophenoxy)acetohydrazide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
B426995-100mg
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$ 70.00 2022-06-07
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$ 230.00 2022-06-07
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SHANG HAI XIAN DING Biotechnology Co., Ltd.
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abcr
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€195.40 2023-02-20
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Chemenu
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Additional information on 2-(2,4-Dibromophenoxy)acetohydrazide

Recent Advances in the Study of 2-(2,4-Dibromophenoxy)acetohydrazide (CAS: 141244-86-2) in Chemical Biology and Pharmaceutical Research

The compound 2-(2,4-Dibromophenoxy)acetohydrazide (CAS: 141244-86-2) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential applications in drug discovery and development. This hydrazide derivative, characterized by its unique bromophenoxy moiety, has been the subject of several studies aimed at elucidating its biological activities, mechanisms of action, and potential therapeutic uses. The following sections provide a comprehensive overview of the latest research findings related to this compound, highlighting its significance in contemporary scientific investigations.

Recent studies have focused on the synthesis and structural optimization of 2-(2,4-Dibromophenoxy)acetohydrazide to enhance its pharmacological properties. Researchers have employed advanced synthetic techniques, including microwave-assisted synthesis and green chemistry approaches, to improve yield and purity. Structural modifications, such as the introduction of additional functional groups, have been explored to increase the compound's bioavailability and target specificity. These efforts have yielded promising results, with several derivatives demonstrating enhanced activity in preliminary biological assays.

In vitro and in vivo studies have revealed that 2-(2,4-Dibromophenoxy)acetohydrazide exhibits notable antimicrobial and anticancer properties. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that the compound effectively inhibits the growth of multidrug-resistant bacterial strains, including methicillin-resistant Staphylococcus aureus (MRSA). The mechanism of action appears to involve disruption of bacterial cell membrane integrity and inhibition of key enzymatic pathways. Additionally, the compound has shown cytotoxic effects against various cancer cell lines, with particular efficacy observed in breast and lung cancer models. These findings suggest its potential as a lead compound for the development of novel antimicrobial and anticancer agents.

Further investigations into the molecular mechanisms underlying the biological activities of 2-(2,4-Dibromophenoxy)acetohydrazide have employed computational modeling and high-throughput screening techniques. Molecular docking studies have identified potential binding interactions with bacterial DNA gyrase and human topoisomerase II, providing insights into its dual antimicrobial and anticancer effects. Moreover, transcriptomic and proteomic analyses have revealed that the compound modulates the expression of genes involved in oxidative stress response and apoptosis, further elucidating its multifaceted pharmacological profile.

Despite these promising findings, challenges remain in the clinical translation of 2-(2,4-Dibromophenoxy)acetohydrazide. Issues such as solubility, stability, and potential toxicity need to be addressed through further preclinical studies. Recent efforts have focused on formulating the compound into nanoparticle-based delivery systems to enhance its pharmacokinetic properties. Preliminary results from animal studies indicate that such formulations can improve bioavailability and reduce off-target effects, paving the way for future clinical trials.

In conclusion, 2-(2,4-Dibromophenoxy)acetohydrazide (CAS: 141244-86-2) represents a promising candidate for drug development, with demonstrated antimicrobial and anticancer activities. Ongoing research aims to optimize its chemical structure, elucidate its mechanisms of action, and overcome translational challenges. The compound's unique properties and versatile applications underscore its potential to contribute significantly to the advancement of chemical biology and pharmaceutical science.

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