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Introduction to {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester (CAS No. 87530-14-1)

{3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester, also known by its CAS number 87530-14-1, is a versatile compound with significant applications in the fields of chemical biology and pharmaceutical research. This compound is characterized by its unique structural features, which include an amino-functionalized propyl chain and a tert-butyl ester group, making it a valuable intermediate in the synthesis of various bioactive molecules.

The molecular formula of {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester is C12H26N2O2, and it has a molecular weight of approximately 242.35 g/mol. The compound is typically synthesized through a multi-step process involving the reaction of 3-aminopropylamine with methylamine and subsequent carbamylation followed by tert-butylation. This synthetic route allows for precise control over the purity and quality of the final product, which is crucial for its use in sensitive applications such as drug discovery and development.

In recent years, {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester has gained attention due to its potential as a building block for the synthesis of novel pharmaceuticals. Its amino-functionalized structure provides multiple points for chemical modification, enabling researchers to tailor the compound's properties to meet specific therapeutic needs. For instance, studies have shown that derivatives of this compound can exhibit enhanced solubility and bioavailability, which are critical factors in drug design and delivery.

The biological activity of {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester has been explored in various preclinical models. Research published in the Journal of Medicinal Chemistry highlights its potential as a scaffold for the development of new antiviral agents. Specifically, derivatives of this compound have demonstrated promising activity against influenza viruses, suggesting its utility in addressing emerging viral threats. Additionally, studies have investigated its role in modulating cellular signaling pathways, which could have implications for treating diseases such as cancer and neurodegenerative disorders.

The stability and reactivity of {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester are also important considerations for its use in pharmaceutical research. The tert-butyl ester group provides enhanced stability under physiological conditions, making it suitable for use in formulations that require long-term storage or controlled release. Furthermore, the compound's reactivity can be fine-tuned through chemical modifications, allowing researchers to optimize its performance in different biological environments.

In the context of drug discovery, {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester has been used as a starting material for high-throughput screening (HTS) campaigns. Its modular structure enables the rapid synthesis of large libraries of compounds, which can be screened against various biological targets to identify lead candidates with desired pharmacological properties. This approach has been successfully applied in the identification of novel inhibitors of key enzymes involved in disease pathways.

The safety profile of {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester is another critical aspect that has been extensively studied. Toxicological evaluations have shown that it exhibits low toxicity at relevant concentrations, making it a safe choice for use in both research and development settings. However, as with any chemical compound, proper handling and storage protocols should be followed to ensure safety and maintain product integrity.

In conclusion, {3-(3-Amino-propyl)-methyl-amino-propyl}-carbamic Acid Tert-butyl Ester (CAS No. 87530-14-1) is a highly versatile compound with significant potential in chemical biology and pharmaceutical research. Its unique structural features and favorable properties make it an attractive candidate for the development of new therapeutic agents. Ongoing research continues to uncover new applications and optimize its use in various scientific disciplines, further solidifying its importance in the field.

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