logo
Home  > Chemistry  > Organic Building Blocks  > Ketones  > 3-Oxo-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester

AB43442

71233-25-5 | 3-Oxo-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $10.00 $7.00 -   +
5g >97% in stock $18.00 $12.00 -   +
10g 97% in stock $23.00 $17.00 -   +
25g 97% in stock $41.00 $29.00 -   +
100g 97% in stock $162.00 $114.00 -   +
500g 97% in stock $808.00 $566.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB43442
Chemical Name: 3-Oxo-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester
CAS Number: 71233-25-5
Molecular Formula: C13H21NO5
Molecular Weight: 271.3095
MDL Number: MFCD09878815
SMILES: CCOC(=O)C1CCN(CC1=O)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 372  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 5  
Undefined Atom Stereocenter Count: 1  
XLogP3: 1.5  

 

 

Upstream Synthesis Route
  • Ethyl 1-N-Boc-3-oxopiperidine-4-carboxylate is a versatile compound widely used in chemical synthesis for its pivotal role in organic chemistry reactions. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials.One key application of Ethyl 1-N-Boc-3-oxopiperidine-4-carboxylate is as a precursor in the synthesis of heterocyclic compounds. Its unique structure provides a valuable starting point for the formation of diverse ring systems, allowing for the development of complex molecules with enhanced biological activities.Furthermore, this compound is frequently employed in the preparation of peptide derivatives, where its functional groups enable selective transformations that are essential for constructing peptide sequences with desired properties. The presence of the Boc (tert-butoxycarbonyl) protecting group ensures the controlled reactivity of the molecule, facilitating specific modifications without undesired side reactions.Overall, Ethyl 1-N-Boc-3-oxopiperidine-4-carboxylate is an indispensable tool in chemical synthesis, offering synthetic chemists a strategic means to access a wide array of structurally diverse and functionally important compounds for various applications across the fields of medicine, agriculture, and materials science.
FEATURED PRODUCTS