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AE11677

1100748-84-2 | 1-Amino-7-azaspiro[3.5]nonane-7-carboxylic acid tert-butyl ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $283.00 $198.00 -   +
1g 95% in stock $589.00 $412.00 -   +
5g 95% in stock $2,159.00 $1,511.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE11677
Chemical Name: 1-Amino-7-azaspiro[3.5]nonane-7-carboxylic acid tert-butyl ester
CAS Number: 1100748-84-2
Molecular Formula: C13H24N2O2
Molecular Weight: 240.3419
MDL Number: MFCD17016205
SMILES: NC1CCC21CCN(CC2)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 301  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • The application of tert-Butyl 1-amino-7-azaspiro[3.5]nonane-7-carboxylate in chemical synthesis lies in its unique structure and functional groups. This compound serves as a versatile building block in organic chemistry, particularly in the synthesis of pharmaceuticals and agrochemicals.Due to its spirocyclic structure, tert-Butyl 1-amino-7-azaspiro[3.5]nonane-7-carboxylate can act as a scaffold for the construction of complex molecular frameworks. Its tert-butyl ester group provides steric hindrance, which can influence the reactivity and selectivity of subsequent chemical reactions. The amino group offers a site for further derivatization, allowing for the introduction of various functional groups to tailor the compound for specific applications.In chemical synthesis, tert-Butyl 1-amino-7-azaspiro[3.5]nonane-7-carboxylate can be utilized for the preparation of bioactive compounds, such as drug candidates or herbicidal agents. Its spirocyclic motif imparts conformational constraints that can enhance the biological activity or pharmacokinetic properties of the final molecules. The presence of the carboxylate group enables the compound to participate in key synthetic transformations, including amidation, esterification, and peptide coupling reactions.Overall, tert-Butyl 1-amino-7-azaspiro[3.5]nonane-7-carboxylate serves as a valuable synthetic intermediate with diverse applications in organic synthesis, medicinal chemistry, and agrochemical research. Its strategic incorporation into molecular design can lead to the development of novel compounds with potential therapeutic or agricultural significance.
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