Cas no 26946-54-3 (Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-)

Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-, is a specialized organic compound featuring a carbohydrazonoyl chloride functional group attached to a benzene ring, further substituted with a 2-chlorophenyl moiety. This structure imparts reactivity suitable for synthesizing heterocyclic compounds, hydrazones, and other derivatives, making it valuable in pharmaceutical and agrochemical research. The presence of the chlorophenyl group enhances its electrophilic character, facilitating nucleophilic substitution reactions. Its stability under controlled conditions allows for precise functionalization in complex synthetic pathways. The compound is typically handled under inert conditions due to its sensitivity to moisture. Its applications include intermediates in medicinal chemistry and materials science, where tailored reactivity is critical.
Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- structure
26946-54-3 structure
Product Name:Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-
CAS No:26946-54-3
MF:C13H10Cl2N2
MW:265.137900829315
CID:250261
PubChem ID:44891157
Update Time:2025-06-09

Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- Chemical and Physical Properties

Names and Identifiers

    • Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-
    • N-(2-CHLOROPHENYL)BENZENECARBOHYDRAZONOYL CHLORIDE
    • Benz-<2-chlor-phenylhydrazid>-chlorid
    • benz<k>aceanthrylene
    • benzoyl chloride 2-chlorophenylhydrazone
    • Benzoylchlorid-2-chlorphenylhydrazin
    • n-(2-chlorophenyl)benzenecarbohydrazonoylchloride
    • 26946-54-3
    • (E)-N-(2-chlorophenyl)benzenecarbohydrazonoyl chloride
    • MFCD09877958
    • MDL: MFCD09877958
    • Inchi: 1S/C13H10Cl2N2/c14-11-8-4-5-9-12(11)16-17-13(15)10-6-2-1-3-7-10/h1-9,16H/b17-13+
    • InChI Key: BOGAULFLMDDDIY-GHRIWEEISA-N
    • SMILES: ClC1C=CC=CC=1N/N=C(\C1C=CC=CC=1)/Cl

Computed Properties

  • Exact Mass: 264.02200
  • Monoisotopic Mass: 264.0221037g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 3
  • Complexity: 262
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 5
  • Topological Polar Surface Area: 24.4?2

Experimental Properties

  • PSA: 24.39000
  • LogP: 4.42550

Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- Security Information

  • Storage Condition:(BD323560)

Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- Customs Data

  • HS CODE:2928000090
  • Customs Data:

    China Customs Code:

    2928000090

    Overview:

    2928000090 Other hydrazine(Hydrazine)And chlorhexidine(hydroxylamine)Organic derivatives of.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Crysdot LLC
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Additional information on Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-

Recent Advances in the Study of Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- (CAS: 26946-54-3)

In recent years, the compound Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- (CAS: 26946-54-3) has garnered significant attention in the field of chemical biology and pharmaceutical research. This compound, characterized by its unique hydrazonoyl chloride moiety and chlorophenyl substitution, has shown promising potential in various applications, including medicinal chemistry, drug discovery, and material science. The latest studies have focused on elucidating its synthesis pathways, biological activities, and potential therapeutic applications, making it a subject of intense scientific inquiry.

One of the key areas of research has been the optimization of synthetic routes for Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-. Recent publications have reported improved methodologies that enhance yield and purity while reducing environmental impact. For instance, a 2023 study published in the Journal of Organic Chemistry demonstrated a novel catalytic approach using palladium-based catalysts, which significantly improved the efficiency of the synthesis process. This advancement not only facilitates large-scale production but also opens new avenues for structural modifications to enhance the compound's bioactivity.

In the realm of medicinal chemistry, Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- has been investigated for its potential as a pharmacophore in drug design. Preliminary in vitro studies have revealed its inhibitory effects on specific enzymes involved in inflammatory pathways, suggesting its utility in developing anti-inflammatory agents. Furthermore, molecular docking simulations have indicated strong binding affinities with target proteins, reinforcing its potential as a lead compound for further drug development. These findings were corroborated by a recent study in Bioorganic & Medicinal Chemistry Letters, which highlighted the compound's selectivity and potency in enzyme inhibition assays.

Beyond its pharmaceutical applications, Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- has also been explored in material science. Researchers have utilized its reactive hydrazonoyl chloride group to synthesize novel polymers with enhanced thermal stability and mechanical properties. A 2022 study in Polymer Chemistry showcased the compound's role in cross-linking reactions, leading to the development of high-performance materials suitable for industrial applications. These interdisciplinary studies underscore the versatility of this compound and its potential to bridge gaps between chemistry, biology, and engineering.

Despite these promising developments, challenges remain in fully harnessing the potential of Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)-. Issues such as scalability, toxicity profiling, and long-term stability need to be addressed to transition from laboratory-scale research to commercial applications. Ongoing studies are focusing on these aspects, with preliminary data indicating favorable outcomes. For example, a recent toxicology report published in Chemical Research in Toxicology found minimal cytotoxicity at therapeutic concentrations, paving the way for further preclinical evaluations.

In conclusion, Benzenecarbohydrazonoylchloride, N-(2-chlorophenyl)- (CAS: 26946-54-3) represents a compound of significant interest in the chemical biology and pharmaceutical sectors. Its diverse applications, from drug discovery to material science, highlight its multifaceted potential. As research progresses, it is anticipated that this compound will play a pivotal role in advancing both scientific understanding and practical innovations in the field. Future studies should continue to explore its mechanistic pathways, optimize its properties, and validate its applications in real-world settings.

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