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AE28101

1067239-08-0 | 1-Boc-3-hydroxypyrrolidine-3-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $85.00 $60.00 -   +
250mg 95% in stock $128.00 $90.00 -   +
500mg 95% in stock $192.00 $134.00 -   +
1g 95% in stock $325.00 $227.00 -   +
5g 95% in stock $944.00 $661.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE28101
Chemical Name: 1-Boc-3-hydroxypyrrolidine-3-carboxylic acid
CAS Number: 1067239-08-0
Molecular Formula: C10H17NO5
Molecular Weight: 231.2457
MDL Number: MFCD15071383
SMILES: O=C(N1CCC(C1)(O)C(=O)O)OC(C)(C)C

 

Computed Properties
Complexity: 309  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • 1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine-3-carboxylic acid, often referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is commonly used as a key intermediate in the preparation of various pharmaceuticals and organic compounds due to its unique chemical properties.One of the primary applications of $name$ in chemical synthesis is as a protecting group in peptide synthesis. By selectively masking the reactive functional groups on amino acids, such as the amine group, $name$ enables precise control over the chemical reactions during peptide assembly. This protection strategy ensures the desired sequence of amino acids is achieved without unwanted side reactions.Additionally, $name$ serves as a valuable starting material for the synthesis of heterocyclic compounds. The presence of the hydroxyl and carboxylic acid functional groups on the pyrrolidine ring allows for further derivatization through a variety of chemical transformations. This versatility makes $name$ a highly useful tool in the construction of complex molecular structures.Furthermore, the tert-butoxycarbonyl (Boc) protecting group on $name$ can be selectively removed under mild conditions, making it a convenient choice for multi-step synthesis processes. This unique feature enhances the synthetic efficiency and overall yield of target molecules.In summary, 1-(tert-Butoxycarbonyl)-3-hydroxypyrrolidine-3-carboxylic acid, or $name$, is a valuable reagent in chemical synthesis, particularly in peptide chemistry and heterocyclic compound synthesis. Its role as a versatile building block underscores its importance in the development of novel pharmaceuticals and organic molecules.
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