Cas no 2228372-09-4 (tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate)

Tert-butyl N-{1-[1-(aminomethyl)-2,2-dimethylcyclopropyl]-2,2-dimethylpropyl}carbamate is a specialized carbamate-protected amine compound featuring a sterically hindered cyclopropane and tert-butyl moiety. Its rigid, highly substituted structure enhances stability, making it suitable for applications requiring controlled reactivity, such as peptide synthesis or pharmaceutical intermediates. The tert-butyloxycarbonyl (Boc) protecting group ensures selective deprotection under mild acidic conditions, while the aminomethyl functionality allows for further derivatization. The compound’s unique cyclopropane ring contributes to conformational constraint, potentially improving binding affinity in drug design. Its high purity and well-defined stereochemistry make it valuable for research in medicinal chemistry and asymmetric synthesis.
tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate structure
2228372-09-4 structure
Product Name:tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate
CAS No:2228372-09-4
MF:C16H32N2O2
MW:284.437484741211
CID:5748808
PubChem ID:165622561
Update Time:2025-05-24

tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate Chemical and Physical Properties

Names and Identifiers

    • 2228372-09-4
    • EN300-1875320
    • tert-butyl N-{1-[1-(aminomethyl)-2,2-dimethylcyclopropyl]-2,2-dimethylpropyl}carbamate
    • tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate
    • Inchi: 1S/C16H32N2O2/c1-13(2,3)11(16(10-17)9-15(16,7)8)18-12(19)20-14(4,5)6/h11H,9-10,17H2,1-8H3,(H,18,19)
    • InChI Key: UYACGJPSBUBRSG-UHFFFAOYSA-N
    • SMILES: O(C(C)(C)C)C(NC(C(C)(C)C)C1(CN)CC1(C)C)=O

Computed Properties

  • Exact Mass: 284.246378268g/mol
  • Monoisotopic Mass: 284.246378268g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 6
  • Complexity: 377
  • 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
  • XLogP3: 3.2
  • Topological Polar Surface Area: 64.4?2

tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate Pricemore >>

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tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate Related Literature

Additional information on tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate

tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate: A Comprehensive Overview

The compound tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate, identified by the CAS number 2228372-09-4, is a complex organic molecule with significant potential in various chemical and pharmaceutical applications. This compound belongs to the class of carbamates, which are widely used in the synthesis of drugs, agrochemicals, and advanced materials. Its structure incorporates a tert-butyl group, a cyclopropane ring, and an amine functionality, making it a versatile building block for further chemical transformations.

Recent studies have highlighted the importance of cyclopropane-containing compounds in drug design due to their unique electronic and steric properties. The presence of a cyclopropane ring in this molecule enhances its stability and bioavailability, making it an attractive candidate for medicinal chemistry applications. Additionally, the amine functionality provides opportunities for further functionalization, such as the formation of amides or ureas, which are crucial in peptide synthesis and drug delivery systems.

The synthesis of tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate involves a multi-step process that combines organocatalytic reactions and transition metal-catalyzed coupling techniques. Researchers have demonstrated that the use of palladium catalysts can significantly improve the yield and selectivity of these reactions. Furthermore, the tert-butyl group serves as an excellent protecting group for sensitive functionalities during the synthesis process.

In terms of applications, this compound has shown promise in the development of novel polymer materials with enhanced mechanical properties. The cyclopropane ring contributes to the rigidity of the polymer backbone, while the amine functionality allows for cross-linking reactions that improve thermal stability and mechanical strength. Recent advancements in polymer chemistry have leveraged such structures to create high-performance materials for use in aerospace and automotive industries.

The biological activity of tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate has also been explored in preclinical studies. Initial assays indicate that this compound exhibits moderate inhibitory activity against certain enzymes involved in inflammatory pathways. Further research is currently underway to optimize its pharmacokinetic properties and evaluate its potential as a therapeutic agent.

In conclusion, tert-butyl N-{1-1-(aminomethyl)-2,2-dimethylcyclopropyl-2,2-dimethylpropyl}carbamate, with its unique structural features and versatile functional groups, represents a valuable addition to the arsenal of chemical tools available to researchers. Its applications span across drug discovery, material science, and advanced chemical synthesis. As ongoing research continues to uncover new insights into its properties and potential uses, this compound is poised to play a significant role in future innovations within these fields.

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