Cas no 162698-26-2 (Methyl Azetidine-2-carboxylate Hydrochloride)

Methyl Azetidine-2-carboxylate Hydrochloride is a versatile heterocyclic building block widely used in organic synthesis and pharmaceutical research. Its strained azetidine ring structure confers unique reactivity, making it valuable for constructing complex molecules, particularly in medicinal chemistry. The hydrochloride salt enhances stability and solubility, facilitating handling and storage. This compound serves as a key intermediate in the synthesis of bioactive compounds, including peptidomimetics and constrained analogs. Its rigid scaffold is advantageous for modulating conformational properties in drug design. The product is typically characterized by high purity, ensuring reproducibility in synthetic applications. Proper storage under anhydrous conditions is recommended to maintain its integrity.
Methyl Azetidine-2-carboxylate Hydrochloride structure
162698-26-2 structure
Product Name:Methyl Azetidine-2-carboxylate Hydrochloride
CAS No:162698-26-2
MF:C5H10ClNO2
MW:151.591400623322
MDL:MFCD01861757
CID:1036748
Update Time:2025-07-01

Methyl Azetidine-2-carboxylate Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • Methyl azetidine-2-carboxylate hydrochloride
    • Methyl 2-azetidinecarboxylate hydrochloride
    • Methyl 2-azetidinecarboxylate HCl
    • METHYL AZETIDINE-2-CARBOXYLATE HCL
    • 2-Azetidinecarboxylic acid, Methyl ester, hydrochloride
    • methyl (2S)-azetidine-2-carboxylate;hydrochloride
    • azetidine-2-carboxylic acid methyl ester hydrochloride
    • FKHBGZKNRAUKEF-UHFFFAOYSA-N
    • SB20436
    • SY013593
    • methyl azetidine-2-carboxylate;hydrochloride
    • ST2407305
    • Azetidine-2-
    • Methyl Azetidine-2-carboxylate Hydrochloride
    • MDL: MFCD01861757
    • Inchi: 1S/C5H9NO2.ClH/c1-8-5(7)4-2-3-6-4;/h4,6H,2-3H2,1H3;1H
    • InChI Key: FKHBGZKNRAUKEF-UHFFFAOYSA-N
    • SMILES: Cl.O(C)C(C1CCN1)=O

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 2
  • Complexity: 103
  • Topological Polar Surface Area: 38.3

Methyl Azetidine-2-carboxylate Hydrochloride Security Information

Methyl Azetidine-2-carboxylate Hydrochloride Pricemore >>

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Additional information on Methyl Azetidine-2-carboxylate Hydrochloride

Comprehensive Overview of Methyl Azetidine-2-carboxylate Hydrochloride (CAS No. 162698-26-2)

Methyl Azetidine-2-carboxylate Hydrochloride (CAS No. 162698-26-2) is a specialized organic compound widely utilized in pharmaceutical research, peptide synthesis, and medicinal chemistry. This hydrochloride salt derivative of Methyl Azetidine-2-carboxylate is valued for its unique structural properties, which facilitate its role as a building block in drug discovery and bioactive molecule development. Researchers and industries increasingly seek this compound due to its potential applications in designing novel therapeutics, particularly in targeting neurological and metabolic disorders.

The growing interest in Methyl Azetidine-2-carboxylate Hydrochloride aligns with broader trends in small molecule drug development and peptide mimetics. As the pharmaceutical industry shifts toward precision medicine, compounds like this are pivotal for creating highly selective inhibitors and receptor modulators. Its azetidine ring structure offers conformational rigidity, enhancing binding affinity in drug-receptor interactions—a feature frequently explored in cancer research and neurodegenerative disease studies.

From a synthetic perspective, Methyl Azetidine-2-carboxylate Hydrochloride serves as a versatile intermediate. Its compatibility with solid-phase peptide synthesis (SPPS) and click chemistry methodologies makes it a preferred choice for structure-activity relationship (SAR) studies. Recent publications highlight its utility in optimizing bioavailability and metabolic stability of lead compounds, addressing common challenges in drug formulation.

Quality and purity are critical for CAS No. 162698-26-2, as impurities can significantly impact experimental outcomes. Reputable suppliers provide analytical certificates (CoA) with detailed HPLC, NMR, and mass spectrometry data to ensure compliance with research standards. Storage recommendations typically include cool, dry conditions (2-8°C) to maintain stability, reflecting its sensitivity to moisture and temperature fluctuations.

Emerging applications of Methyl Azetidine-2-carboxylate Hydrochloride extend to prodrug design and bioconjugation strategies. Its carboxylic ester group allows for facile derivatization, enabling researchers to engineer targeted drug delivery systems. This adaptability resonates with current demands for personalized therapeutics and sustainable chemistry practices, where efficient molecular modifications reduce waste and improve efficacy.

For those sourcing Methyl Azetidine-2-carboxylate Hydrochloride, understanding regulatory compliance is essential. While not classified as hazardous under standard protocols, proper laboratory handling (e.g., gloves, ventilation) is advised. The compound's CAS No. 162698-26-2 is frequently indexed in scientific databases like SciFinder and Reaxys, underscoring its relevance in contemporary research workflows.

In summary, Methyl Azetidine-2-carboxylate Hydrochloride represents a critical tool for advancing medicinal chemistry and pharmaceutical innovation. Its multifaceted applications—from peptide backbone modifications to enzyme inhibitor design—position it at the forefront of cutting-edge research. As scientific inquiries into protein-protein interactions and allosteric modulation expand, this compound will likely remain a cornerstone in developing next-generation therapeutics.

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