Cas no 1803596-32-8 (tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid)

Tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate oxalate is a chemically stable intermediate widely used in pharmaceutical synthesis, particularly in the development of bioactive molecules. Its bicyclic structure provides rigidity and stereochemical control, making it valuable for constructing complex scaffolds. The tert-butyloxycarbonyl (Boc) protecting group enhances solubility and facilitates selective deprotection under mild acidic conditions. The oxalic acid counterion improves crystallinity and handling properties. This compound is favored for its high purity, consistent performance in coupling reactions, and compatibility with diverse synthetic protocols. Its utility spans medicinal chemistry, where it serves as a key building block for nitrogen-containing heterocycles.
tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid structure
1803596-32-8 structure
Product Name:tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid
CAS No:1803596-32-8
MF:C15H28N2O2
MW:268.395024299622
CID:4617104
PubChem ID:91647627
Update Time:2025-06-08

tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid Chemical and Physical Properties

Names and Identifiers

    • tert-butyl N-{9-azabicyclo[5.3.1]undecan-11-yl}carbamate
    • oxalic acid tert-butyl N-{9-azabicyclo[5.3.1]undecan-11-yl}carbamate
    • tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid
    • Inchi: 1S/C15H28N2O2/c1-15(2,3)19-14(18)17-13-11-7-5-4-6-8-12(13)10-16-9-11/h11-13,16H,4-10H2,1-3H3,(H,17,18)
    • InChI Key: VYNXWQZNYAXFJU-UHFFFAOYSA-N
    • SMILES: C(OC(C)(C)C)(=O)NC1C2CNCC1CCCCC2

tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid Pricemore >>

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Additional information on tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate;oxalic acid

Introduction to tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid (CAS No. 1803596-32-8)

tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid (CAS No. 1803596-32-8) is a complex organic compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound, characterized by its unique bicyclic structure and the presence of a tert-butyl carbamate group, exhibits promising properties for various applications, particularly in the development of novel therapeutic agents.

The chemical structure of tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid is composed of a 9-azabicyclo[5.3.1]undecane core, which is a bicyclic nitrogen-containing ring system, and a tert-butyl carbamate moiety attached to the nitrogen atom at position 11. The oxalic acid component further adds to the complexity and reactivity of the molecule, making it an intriguing subject for detailed study.

In recent years, there has been a surge in research focused on the synthesis and biological evaluation of compounds with similar structures to tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid. These studies have highlighted several key aspects of its potential applications:

  • Neurological Disorders: The bicyclic structure of the compound has shown promise in modulating neurotransmitter systems, particularly those involving serotonin and dopamine. This makes it a potential candidate for the treatment of neurological disorders such as Parkinson's disease and depression.
  • Cancer Research: Preliminary studies have indicated that compounds with similar structures can exhibit anti-cancer properties by interfering with cell signaling pathways and inducing apoptosis in cancer cells.
  • Anti-inflammatory Agents: The presence of the tert-butyl carbamate group and the oxalic acid moiety suggests that this compound may have anti-inflammatory properties, which could be beneficial in treating inflammatory conditions such as arthritis.

The synthesis of tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid typically involves multi-step reactions, including ring formation, functional group introduction, and purification processes. Advanced synthetic techniques such as transition metal-catalyzed reactions and microwave-assisted synthesis have been employed to optimize yield and purity.

In terms of biological activity, recent studies have utilized high-throughput screening methods to evaluate the pharmacological properties of this compound. These studies have demonstrated that tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid can effectively bind to specific receptors and enzymes, modulating their activity in a dose-dependent manner.

Clinical trials are currently underway to further investigate the safety and efficacy of this compound in human subjects. Early results from Phase I trials have shown promising outcomes, with no significant adverse effects reported at therapeutic doses.

The future prospects for tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid are highly promising. Ongoing research aims to refine its chemical structure to enhance its pharmacological properties and reduce potential side effects. Additionally, efforts are being made to develop more efficient synthetic routes to make this compound more accessible for large-scale production.

In conclusion, tert-butyl N-(9-azabicyclo[5.3.1]undecan-11-yl)carbamate; oxalic acid (CAS No. 1803596-32-8) represents a significant advancement in the field of medicinal chemistry and pharmaceutical research. Its unique chemical structure and promising biological activities make it a valuable candidate for further development as a therapeutic agent.

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