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876317-19-0

1-(tert-Butoxycarbonyl)-4-oxopyrrolidine-2-carboxylicacid

Catalog#: AR00372A  |   CAS#: 876317-19-0  |   MDL#: MFCD02668169  |   MF: C10H15NO5  |   MW: 229.2298

Packsize Purity Price Availability Quantity
100mg 97% $4.00 Global Stock Buy Now Add To Cart
250mg 97% $6.00 Global Stock Buy Now Add To Cart
1g 97% $12.00 Global Stock Buy Now Add To Cart
5g 97% $52.00 Global Stock Buy Now Add To Cart
10g 97% $97.00 Global Stock Buy Now Add To Cart
25g 97% $236.00 Global Stock Buy Now Add To Cart
100g 97% $779.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00372A
Chemical Name 1-(tert-Butoxycarbonyl)-4-oxopyrrolidine-2-carboxylicacid
CAS Number 876317-19-0
Molecular Formula C10H15NO5
Molecular Weight 229.2298
MDL Number MFCD02668169
SMILES O=C1CN(C(C1)C(=O)O)C(=O)OC(C)(C)C

1-(tert-Butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acid, also known as $name$, is a versatile compound widely used in chemical synthesis. Its primary application lies in its role as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals.In the realm of chemical synthesis, $name$ serves as a valuable building block due to its unique structural properties. This compound can undergo a range of chemical reactions, such as nucleophilic additions, acylations, and cyclizations, to generate structurally diverse molecules. Its presence in the molecular structure can impart specific functionalities or stereochemical characteristics that are crucial for the desired biological activity or chemical properties of the final product.Moreover, the tert-butoxycarbonyl (Boc) protecting group in $name$ plays a pivotal role in controlling the reactivity and selectivity of subsequent reactions. By selectively masking reactive functional groups within a molecule, the Boc group allows chemists to carry out multi-step synthetic sequences with precision and efficiency. Upon completion of the desired transformations, the Boc group can be readily removed under mild conditions to reveal the free amine group, enabling further elaboration of the molecule.In summary, the strategic incorporation of 1-(tert-Butoxycarbonyl)-4-oxopyrrolidine-2-carboxylic acid in chemical synthesis enables access to intricate molecular architectures with tailored properties. Its application extends to the synthesis of complex organic compounds with biological, medicinal, and material science relevance.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H332-H335
Precautionary Statements P261-P280-P305+P351+P338
Class N/A
Packing Group N/A

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