Cas no 94126-97-3 (2,5-Pyridinedi(methylchloride))

2,5-Pyridinedi(methylchloride) is a versatile bifunctional reagent featuring reactive chloromethyl groups at the 2 and 5 positions of the pyridine ring. This compound serves as a valuable intermediate in organic synthesis, particularly for constructing heterocyclic frameworks and functionalized pyridine derivatives. Its dual electrophilic sites enable efficient cross-coupling or nucleophilic substitution reactions, facilitating the introduction of diverse substituents. The pyridine core enhances stability while allowing further derivatization. Applications include pharmaceutical synthesis, ligand design, and polymer modification. The compound’s high reactivity and well-defined structure make it suitable for controlled functionalization in complex molecular architectures. Proper handling under inert conditions is recommended due to its moisture sensitivity.
2,5-Pyridinedi(methylchloride) structure
94126-97-3 structure
Product Name:2,5-Pyridinedi(methylchloride)
CAS No:94126-97-3
MF:C7H7Cl2N
MW:176.043179750443
CID:1063270
PubChem ID:13221020
Update Time:2025-11-02

2,5-Pyridinedi(methylchloride) Chemical and Physical Properties

Names and Identifiers

    • 2,5-Pyridinedi(methylchloride)
    • 2,5-bis(chloromethyl)pyridine
    • DTXSID40529402
    • EN300-7431373
    • SCHEMBL4135195
    • 94126-97-3
    • Pyridine, 2,5-bis(chloromethyl)-
    • starbld0002948
    • Inchi: 1S/C7H7Cl2N/c8-3-6-1-2-7(4-9)10-5-6/h1-2,5H,3-4H2
    • InChI Key: OMOWJNFBJPIHDM-UHFFFAOYSA-N
    • SMILES: ClCC1=CN=C(CCl)C=C1

Computed Properties

  • Exact Mass: 174.9955546g/mol
  • Monoisotopic Mass: 174.9955546g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 97.6
  • 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: 1.7
  • Topological Polar Surface Area: 12.9?2

2,5-Pyridinedi(methylchloride) Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
P991815-100mg
2,5-Pyridinedi(methylchloride)
94126-97-3
100mg
$207.00 2023-05-17
TRC
P991815-1g
2,5-Pyridinedi(methylchloride)
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$1642.00 2023-05-17
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AR005VGU-50mg
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$340.00 2025-02-13
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AR005VGU-100mg
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100mg
$496.00 2025-02-13
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AR005VGU-250mg
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$695.00 2025-02-13
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AR005VGU-500mg
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$1081.00 2025-02-13
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$1381.00 2025-02-13
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AR005VGU-2.5g
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AR005VGU-5g
Pyridine, 2,5-bis(chloromethyl)-
94126-97-3 95%
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$3955.00 2024-07-18
Aaron
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2,5-Pyridinedi(methylchloride) Related Literature

Additional information on 2,5-Pyridinedi(methylchloride)

2,5-Pyridinedi(methylchloride) (CAS No. 94126-97-3): Properties, Applications, and Industry Insights

2,5-Pyridinedi(methylchloride) (CAS No. 94126-97-3) is a specialized organic compound with significant relevance in modern chemical research and industrial applications. This heterocyclic derivative, featuring a pyridine core with two chloromethyl substituents at the 2 and 5 positions, has garnered attention for its versatile reactivity and utility in synthetic chemistry. The compound's molecular formula, C7H7Cl2N, and its distinct structural features make it a valuable intermediate in the synthesis of more complex molecules.

The chemical properties of 2,5-Pyridinedi(methylchloride) are characterized by its reactivity, particularly in nucleophilic substitution reactions. The presence of two chloromethyl groups on the pyridine ring allows for diverse functionalization, enabling the creation of various derivatives. Researchers often explore its potential in pharmaceutical intermediates and agrochemical synthesis, where its structural motifs are highly sought after. Recent trends in green chemistry have also spurred interest in optimizing its synthesis to minimize environmental impact.

One of the most notable applications of 2,5-Pyridinedi(methylchloride) is in the development of advanced materials. Its ability to act as a cross-linking agent or a precursor for polymeric structures has made it valuable in fields such as coating technologies and electronic materials. With the growing demand for high-performance polymers, this compound has found its way into research on conductive polymers and nanomaterials, aligning with the industry's shift toward sustainable and efficient material solutions.

Market dynamics for 2,5-Pyridinedi(methylchloride) (CAS 94126-97-3) reflect its niche yet expanding role in specialty chemicals. The compound's supply chain is influenced by factors such as raw material availability and regulatory compliance. Industry reports suggest an uptick in demand from the pharmaceutical sector, where it serves as a key intermediate in drug discovery. Additionally, the rise of custom synthesis services has facilitated easier access to this compound for research institutions and smaller enterprises.

From a safety and handling perspective, proper storage conditions for 2,5-Pyridinedi(methylchloride) include protection from moisture and extreme temperatures. While not classified under stringent hazardous categories, standard laboratory precautions should be observed during its use. Researchers frequently inquire about compatibility with other reagents and stability under various conditions, topics that remain central to its practical applications.

Innovations in synthetic methodologies have further enhanced the appeal of 2,5-Pyridinedi(methylchloride). Recent publications highlight its role in catalyzed reactions and multi-step syntheses, demonstrating its adaptability in modern organic chemistry. The compound's compatibility with microwave-assisted synthesis and flow chemistry techniques has also been explored, catering to the industry's push for faster and more efficient processes.

Looking ahead, the future of 2,5-Pyridinedi(methylchloride) appears promising, with potential expansions into bioconjugation chemistry and medicinal chemistry applications. Its structural versatility ensures continued relevance in both academic and industrial settings. As researchers uncover new reaction pathways and applications, this compound is poised to remain a staple in the toolkit of synthetic chemists worldwide.

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