Cas no 860297-27-4 (2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE)

2-(BOC-Amino)-cyclopentanemethanamine is a protected amine derivative featuring a cyclopentane backbone with a Boc (tert-butoxycarbonyl) group and a primary amine functionality. This compound is valuable in organic synthesis, particularly in peptide and pharmaceutical chemistry, where selective amine protection is required. The Boc group provides stability under basic conditions and can be readily removed under acidic conditions, enabling controlled deprotection in multi-step syntheses. Its cyclopentane structure offers conformational rigidity, which can influence stereochemical outcomes in reactions. The compound is commonly used as an intermediate in the preparation of bioactive molecules, making it a useful building block for medicinal chemistry and drug development.
2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE structure
860297-27-4 structure
Product Name:2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE
CAS No:860297-27-4
MF:C11H22N2O2
MW:214.304583072662
MDL:MFCD21364671
CID:1849819
PubChem ID:72942848
Update Time:2025-08-05

2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE Chemical and Physical Properties

Names and Identifiers

    • 2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE
    • tert-butyl N-[2-(aminomethyl)cyclopentyl]carbamate
    • HGRDDBPZHZEGNY-BDAKNGLRSA-N
    • 860297-27-4
    • D74267
    • CS-0080998
    • AKOS022179876
    • tert-butyl(1S,2R)-2-(aminomethyl)cyclopentylcarbamate
    • tert-Butyl ((1S,2R)-2-(aminomethyl)cyclopentyl)carbamate
    • MFCD21364671
    • Tert-butyl [(1S,2R)-2-(aminomethyl)cyclopentyl]carbamate
    • TERT-BUTYL N-[(1S,2R)-2-(AMINOMETHYL)CYCLOPENTYL]CARBAMATE
    • MDL： MFCD21364671
    • Inchi： 1S/C11H22N2O2/c1-11(2,3)15-10(14)13-9-6-4-5-8(9)7-12/h8-9H,4-7,12H2,1-3H3,(H,13,14)/t8-,9+/m1/s1
    • InChI Key： HGRDDBPZHZEGNY-BDAKNGLRSA-N
    • SMILES： O(C(C)(C)C)C(N[C@H]1CCC[C@@H]1CN)=O

Computed Properties

  • Exact Mass: 214.168
  • Monoisotopic Mass: 214.168
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 4
  • Complexity: 223
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 64.4A^2
  • XLogP3: 1.7

Experimental Properties

  • LogP: 2.54320

2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE Pricemore >>

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tert-Butyl N-[(1S,2R)-2-(aminomethyl)cyclopentyl]carbamate; .
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2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE Related Literature

Additional information on 2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE

Comprehensive Overview of 2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE (CAS No. 860297-27-4): Properties, Applications, and Industry Insights

2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE (CAS No. 860297-27-4) is a specialized BOC-protected amine derivative widely utilized in pharmaceutical synthesis and organic chemistry. This compound features a cyclopentane backbone with a BOC (tert-butoxycarbonyl) protecting group, making it a versatile intermediate for peptide coupling, drug discovery, and chiral synthesis. Its molecular structure (C11H22N2O2) and stereochemical properties have garnered significant attention from researchers exploring novel bioactive molecules.

In recent years, the demand for high-purity chiral building blocks like 2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE has surged due to advancements in targeted drug delivery and small-molecule therapeutics. Industry trends show increased searches for "BOC-amine applications" and "CAS 860297-27-4 solubility," reflecting its relevance in optimizing reaction yields and green chemistry protocols. The compound’s stability under acidic conditions (via BOC deprotection) further enhances its utility in multistep syntheses.

From an SEO perspective, key queries such as "buy 2-(BOC-AMINO)-CYCLOPENTANEMETHANAMINE" and "860297-27-4 synthesis protocol" highlight commercial and academic interest. Analytical data reveals its compatibility with HPLC purification (typically >95% purity) and solubility in polar aprotic solvents like DMF or DMSO. Researchers also frequently inquire about "BOC vs. Fmoc protection" comparisons, where this compound’s selective deprotection advantages are often emphasized.

Environmental and regulatory considerations are increasingly shaping its use. The compound aligns with sustainable chemistry principles due to its minimal byproduct generation during BOC removal. Recent publications discuss its role in bioconjugation techniques for antibody-drug conjugates (ADCs), a hotspot in oncology research. Notably, its low toxicity profile (per OECD guidelines) makes it preferable for GMP-grade applications.

Future prospects for CAS 860297-27-4 include expanded use in asymmetric catalysis and protease inhibitor development. Patent analyses indicate growing IP filings involving its cyclopentane scaffold for metabolic disease therapeutics. As synthetic methodologies evolve, this compound remains a critical tool for addressing challenges in stereoselective synthesis and peptide mimetics design.

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