Cas no 52208-56-7 (3-Chloro-2,6-difluoropyridine)

3-Chloro-2,6-difluoropyridine structure
3-Chloro-2,6-difluoropyridine structure
Product Name:3-Chloro-2,6-difluoropyridine
CAS No:52208-56-7
MF:C5H2ClF2N
MW:149.525887012482
MDL:MFCD11044285
CID:936572
PubChem ID:12259371
Update Time:2025-07-21

3-Chloro-2,6-difluoropyridine Chemical and Physical Properties

Names and Identifiers

    • 3-Chloro-2,6-difluoropyridine
    • 2,6-Difluor-3-chlor-pyridin
    • 2,6-difluoro-5-chloropyridine
    • 3-Chloro-2,6-difluoro-pyridine
    • 2,6-Difluoro-3-chloropyridine
    • Pyridine, 3-chloro-2,6-difluoro-
    • 4869AE
    • A26148
    • D82210
    • SB53456
    • AMY12492
    • BS-28615
    • DTXSID80482805
    • CS-0156789
    • 52208-56-7
    • MFCD11044285
    • SCHEMBL432833
    • AKOS006307332
    • DB-082211
    • SY047823
    • EN300-309216
    • DTXCID80433615
    • MDL: MFCD11044285
    • Inchi: 1S/C5H2ClF2N/c6-3-1-2-4(7)9-5(3)8/h1-2H
    • InChI Key: BABNLQDXRCOTJA-UHFFFAOYSA-N
    • SMILES: ClC1C(=NC(=CC=1)F)F

Computed Properties

  • Exact Mass: 148.98400
  • Monoisotopic Mass: 148.9843831g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 0
  • Complexity: 101
  • 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
  • Topological Polar Surface Area: 12.9
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2.3

Experimental Properties

  • PSA: 12.89000
  • LogP: 2.01320

3-Chloro-2,6-difluoropyridine Security Information

  • HazardClass:IRRITANT

3-Chloro-2,6-difluoropyridine Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Additional information on 3-Chloro-2,6-difluoropyridine

Comprehensive Overview of 3-Chloro-2,6-difluoropyridine (CAS No. 52208-56-7): Properties, Applications, and Industry Insights

3-Chloro-2,6-difluoropyridine (CAS No. 52208-56-7) is a halogenated pyridine derivative that has garnered significant attention in the pharmaceutical and agrochemical industries due to its versatile reactivity and structural properties. This compound, characterized by its chloro and difluoro substitutions, serves as a critical intermediate in the synthesis of advanced molecules. Its unique heterocyclic framework makes it a valuable building block for researchers exploring crop protection agents, pharmaceutical intermediates, and material science innovations.

The growing demand for 3-Chloro-2,6-difluoropyridine is closely tied to its role in developing next-generation pesticides and drug candidates. With increasing global focus on sustainable agriculture, this compound is often highlighted in discussions about low-residue agrochemicals. Its ability to act as a precursor for selective herbicides aligns with the industry’s shift toward environmentally friendly solutions. Additionally, its applications in medicinal chemistry—particularly in the design of fluorinated APIs (Active Pharmaceutical Ingredients)—reflect broader trends favoring bioavailability enhancement and metabolic stability in drug development.

From a chemical perspective, 52208-56-7 exhibits notable stability under standard conditions, with a molecular formula of C5H2ClF2N. Its electron-withdrawing substituents facilitate nucleophilic aromatic substitution reactions, a feature widely exploited in custom synthesis workflows. Researchers frequently search for synthetic protocols involving this compound, underscoring its utility in cross-coupling reactions and catalysis. Recent publications have also explored its potential in OLED materials, linking it to advancements in flexible electronics—a hot topic in materials science forums.

Quality control and analytical standards for 3-Chloro-2,6-difluoropyridine are critical considerations for manufacturers. Techniques like HPLC, GC-MS, and NMR spectroscopy are routinely employed to verify purity, which typically exceeds 98% for commercial grades. The compound’s storage conditions (often recommended at 2–8°C under inert atmospheres) and handling precautions are frequently queried in chemical databases, reflecting end-user concerns about long-term stability.

In the context of regulatory compliance, 52208-56-7 is not classified under restricted categories, making it accessible for research and industrial use. However, its halogenated nature prompts discussions on green chemistry alternatives, such as solvent-free synthesis or catalytic fluorination methods. These topics resonate with the sustainability-driven agendas of modern chemical enterprises.

Market analysts project steady growth for 3-Chloro-2,6-difluoropyridine, driven by its expanding applications in crop science and pharmaceutical R&D. Patent filings reveal its incorporation into novel fungicides and kinase inhibitors, further solidifying its industrial relevance. For procurement specialists, understanding supply chain dynamics—including regional production hubs in Asia and Europe—is essential to mitigate raw material shortages.

In summary, 3-Chloro-2,6-difluoropyridine (CAS No. 52208-56-7) stands at the intersection of innovation and practical utility. Its multifaceted roles in agrochemicals, pharmaceuticals, and emerging technologies make it a compound of enduring interest. As industries prioritize efficiency and sustainability, this pyridine derivative will likely remain a cornerstone of specialty chemical development.

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