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Home  > Azetidine-1,2-dicarboxylic acid 1-tert-butyl ester

AA81943

159749-28-7 | Azetidine-1,2-dicarboxylic acid 1-tert-butyl ester

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $12.00 $9.00 -   +
5g 97% in stock $33.00 $24.00 -   +
10g 97% in stock $54.00 $38.00 -   +
25g 97% in stock $132.00 $93.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA81943
Chemical Name: Azetidine-1,2-dicarboxylic acid 1-tert-butyl ester
CAS Number: 159749-28-7
Molecular Formula: C9H15NO4
Molecular Weight: 201.2197
MDL Number: MFCD01861756
SMILES: O=C(N1CCC1C(=O)O)OC(C)(C)C

 

Computed Properties
Complexity: 256  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 1-(tert-Butoxycarbonyl)azetidine-2-carboxylic acid, commonly referred to as $name$, is a valuable compound widely used in chemical synthesis for its unique properties and versatile applications. This compound plays a crucial role as a protecting group in peptide synthesis, a key process in the production of various bioactive molecules and pharmaceuticals.In chemical synthesis, $name$ serves as a protective agent that shields specific functional groups within a molecule, allowing selective reactions to take place without interference from other reactive sites. By introducing the tert-Butoxycarbonyl (Boc) group to the azetidine-2-carboxylic acid moiety, this compound effectively masks the carboxylic acid functionality, enabling controlled modifications and manipulations in subsequent synthetic steps.Moreover, the Boc protecting group in $name$ is easily removable under mild acidic conditions, facilitating its cleavage and the regeneration of the original functional groups. This reversibility feature is essential in organic synthesis, as it enables the precise manipulation of molecular structures and the synthesis of complex molecules with high efficiency and selectivity.Overall, the application of 1-(tert-Butoxycarbonyl)azetidine-2-carboxylic acid as a protecting group in chemical synthesis offers chemists a valuable tool for the efficient and controlled assembly of diverse molecules, making it an indispensable component in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.
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