Cas no 926205-46-1 (2-(4-methylpiperidin-1-yl)pyridin-3-amine)

2-(4-Methylpiperidin-1-yl)pyridin-3-amine is a heterocyclic compound featuring both pyridine and piperidine moieties, which impart unique chemical properties. The 4-methylpiperidin-1-yl substituent enhances steric and electronic effects, influencing reactivity and binding interactions. This structure is valuable in pharmaceutical and agrochemical research, particularly as a building block for bioactive molecules. Its amine functionality offers versatility for further derivatization, enabling the synthesis of diverse analogs. The compound’s stability and moderate polarity make it suitable for applications in medicinal chemistry, where it may serve as an intermediate in the development of receptor-targeted agents. Careful handling is advised due to potential sensitivity to air or moisture.
2-(4-methylpiperidin-1-yl)pyridin-3-amine structure
926205-46-1 structure
Product Name:2-(4-methylpiperidin-1-yl)pyridin-3-amine
CAS No:926205-46-1
MF:C11H17N3
MW:191.272782087326
MDL:MFCD08700154
CID:1072374
PubChem ID:16773072
Update Time:2025-06-10

2-(4-methylpiperidin-1-yl)pyridin-3-amine Chemical and Physical Properties

Names and Identifiers

    • 2-(4-Methyl-1-piperidinyl)-3-pyridinylamine
    • F1907-0361
    • 2-(4-Methyl-1-piperidinyl)-3-pyridinamine
    • DTXSID701271487
    • 2-(4-methylpiperidin-1-yl)pyridin-3-amine
    • EN300-265472
    • SB41505
    • AKOS000129129
    • BMB20546
    • SCHEMBL6219881
    • 926205-46-1
    • MDL: MFCD08700154
    • Inchi: 1S/C11H17N3/c1-9-4-7-14(8-5-9)11-10(12)3-2-6-13-11/h2-3,6,9H,4-5,7-8,12H2,1H3
    • InChI Key: JNBHCONHFUNVNI-UHFFFAOYSA-N
    • SMILES: N1(C2C(=CC=CN=2)N)CCC(C)CC1

Computed Properties

  • Exact Mass: 191.142247555g/mol
  • Monoisotopic Mass: 191.142247555g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 175
  • 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: 42.2?2

2-(4-methylpiperidin-1-yl)pyridin-3-amine Pricemore >>

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Additional information on 2-(4-methylpiperidin-1-yl)pyridin-3-amine

Recent Advances in the Study of 2-(4-methylpiperidin-1-yl)pyridin-3-amine (CAS: 926205-46-1)

2-(4-methylpiperidin-1-yl)pyridin-3-amine (CAS: 926205-46-1) is a chemical compound that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential therapeutic applications. Recent studies have focused on elucidating its pharmacological properties, synthetic pathways, and mechanisms of action, particularly in the context of drug discovery and development. This research brief aims to provide an overview of the latest findings related to this compound, highlighting its significance in current scientific endeavors.

The compound, characterized by its pyridine and piperidine moieties, has been investigated for its role as a building block in the synthesis of more complex molecules. Researchers have explored its utility in the development of kinase inhibitors, which are crucial for targeting various signaling pathways implicated in diseases such as cancer and inflammatory disorders. The structural flexibility of 2-(4-methylpiperidin-1-yl)pyridin-3-amine allows for modifications that can enhance its binding affinity and selectivity towards specific biological targets.

Recent publications have detailed innovative synthetic routes to produce 2-(4-methylpiperidin-1-yl)pyridin-3-amine with high yield and purity. These methods often involve multi-step reactions, including amination and cyclization processes, which are optimized to minimize by-products and improve scalability. Advances in catalytic systems and green chemistry principles have further refined these synthetic approaches, making them more efficient and environmentally friendly.

In vitro and in vivo studies have demonstrated the compound's potential as a modulator of key enzymatic activities. For instance, it has shown promising results in inhibiting specific kinases involved in cell proliferation and survival. These findings are supported by detailed structural-activity relationship (SAR) analyses, which provide insights into how modifications to the compound's core structure can influence its biological activity. Such studies are instrumental in guiding the design of next-generation therapeutics.

Despite these advancements, challenges remain in translating the preclinical findings into clinical applications. Issues such as bioavailability, metabolic stability, and potential off-target effects need to be addressed through further research. Collaborative efforts between academic institutions and pharmaceutical companies are essential to overcome these hurdles and accelerate the development of 2-(4-methylpiperidin-1-yl)pyridin-3-amine-based drugs.

In conclusion, 2-(4-methylpiperidin-1-yl)pyridin-3-amine represents a promising scaffold in medicinal chemistry, with ongoing research uncovering its diverse applications. The compound's versatility and the continuous refinement of its synthetic and pharmacological profiles underscore its potential to contribute significantly to the development of novel therapeutics. Future studies should focus on optimizing its properties and exploring its efficacy in more complex biological systems.

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