AE28101
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.
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 |
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 |
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.