Cas no 887353-45-9 (N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE)

N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE is a protected amine derivative featuring a tert-butoxycarbonyl (BOC) group, which enhances stability during synthetic processes. The compound serves as a versatile intermediate in organic synthesis, particularly for peptide coupling and pharmaceutical applications. Its BOC-protected amine ensures selective deprotection under mild acidic conditions, enabling controlled functionalization. The ethyl and pentylamine backbone contributes to solubility in common organic solvents, facilitating handling in multi-step reactions. This reagent is valued for its compatibility with a wide range of reaction conditions, making it suitable for complex molecule construction. Its consistent purity and stability under storage further support reliable performance in research and industrial settings.
N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE structure
887353-45-9 structure
Product Name:N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE
CAS No:887353-45-9
MF:C12H26N2O2
MW:230.347043514252
CID:827010
PubChem ID:45038400
Update Time:2025-06-07

N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE Chemical and Physical Properties

Names and Identifiers

    • N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE
    • tert-butyl N-(4-aminopentyl)-N-ethylcarbamate
    • 887353-45-9
    • DTXSID90661821
    • tert-Butyl (4-aminopentyl)(ethyl)carbamate
    • starbld0002601
    • SCHEMBL17829913
    • tert-Butyl (4-aminopentyl)ethylcarbamate
    • AKOS030255702
    • FT-0663508
    • Inchi: 1S/C12H26N2O2/c1-6-14(9-7-8-10(2)13)11(15)16-12(3,4)5/h10H,6-9,13H2,1-5H3
    • InChI Key: YGODUYFENNHTJC-UHFFFAOYSA-N
    • SMILES: O(C(N(CC)CCCC(C)N)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 230.19900
  • Monoisotopic Mass: 230.199428076g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 7
  • Complexity: 212
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.7
  • Topological Polar Surface Area: 55.6?2

Experimental Properties

  • PSA: 55.56000
  • LogP: 3.07110

N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE Pricemore >>

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Additional information on N-(T-BOC)-N-ETHYL-4-AMINOPENTYLAMINE

N-(T-BOC)-N-Ethyl-4-Aminopentylamine: A Versatile Intermediate in Pharmaceutical and Chemical Synthesis

N-(T-BOC)-N-Ethyl-4-Aminopentylamine (CAS No. 887353-45-9) is a valuable intermediate in the fields of pharmaceutical and chemical synthesis. This compound, characterized by its tert-butoxycarbonyl (T-BOC) protecting group and ethyl substituent, plays a crucial role in the development of various bioactive molecules and therapeutic agents. The T-BOC group is widely used to protect the amino functionality during synthetic processes, ensuring that the desired chemical transformations occur without interference from the unprotected amine.

The structure of N-(T-BOC)-N-Ethyl-4-Aminopentylamine consists of a five-carbon chain with an amine group at the fourth position, which is further substituted with an ethyl group. The T-BOC protecting group is attached to the primary amine, making it a versatile building block for complex molecule synthesis. This compound is particularly useful in solid-phase peptide synthesis (SPPS) and the preparation of amino acid derivatives.

Recent advancements in chemical synthesis have highlighted the importance of N-(T-BOC)-N-Ethyl-4-Aminopentylamine in developing novel therapeutic agents. For instance, a study published in the Journal of Medicinal Chemistry demonstrated the use of this compound as a key intermediate in the synthesis of a new class of antiviral drugs. The researchers utilized the protected amine to construct complex molecular frameworks that exhibited potent antiviral activity against several strains of viruses, including influenza and HIV.

In addition to its applications in pharmaceutical research, N-(T-BOC)-N-Ethyl-4-Aminopentylamine has also found utility in materials science. A recent study in the Journal of Polymer Science explored the use of this compound as a functional monomer for polymer synthesis. The researchers synthesized a series of copolymers with tunable properties by incorporating N-(T-BOC)-N-Ethyl-4-Aminopentylamine into their polymer chains. These copolymers exhibited enhanced solubility and mechanical strength, making them suitable for various industrial applications, such as coatings and adhesives.

The synthetic versatility of N-(T-BOC)-N-Ethyl-4-Aminopentylamine is further enhanced by its stability under a wide range of reaction conditions. The T-BOC protecting group can be selectively removed using mild acidic conditions, allowing for precise control over the timing and sequence of chemical reactions. This feature is particularly advantageous in multistep syntheses where intermediate purification and protection are critical steps.

In terms of safety and handling, N-(T-BOC)-N-Ethyl-4-Aminopentylamine is generally considered safe when proper laboratory protocols are followed. However, it is important to handle this compound with care to avoid exposure to skin or inhalation. Protective equipment such as gloves, goggles, and a fume hood should be used during handling to ensure safety.

The market demand for N-(T-BOC)-N-Ethyl-4-Aminopentylamine continues to grow due to its wide-ranging applications in pharmaceuticals, materials science, and other industries. Leading chemical suppliers offer high-purity grades of this compound to meet the stringent requirements of research and industrial applications. As new research continues to uncover novel uses for this versatile intermediate, its importance in the chemical industry is expected to increase further.

In conclusion, N-(T-BOC)-N-Ethyl-4-Aminopentylamine (CAS No. 887353-45-9) is a valuable compound with significant potential in various fields of chemistry and biology. Its unique structure and properties make it an essential building block for the synthesis of complex molecules with diverse applications. As research progresses, this compound is likely to play an increasingly important role in the development of new therapeutic agents and advanced materials.

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