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65595-02-0

3-[(2S)-1-[(tert-butoxy)carbonyl]pyrrolidin-2-yl]propanoic acid

Catalog#: AR01A3KC  |   CAS#: 65595-02-0  |   MDL#: MFCD11226805  |   MF: C12H21NO4  |   MW: 243.2994

Packsize Purity Price Availability Quantity
50mg 95% $232.00 2-3 weeks Buy Now Add To Cart
100mg 95% $333.00 2-3 weeks Buy Now Add To Cart
250mg 95% $463.00 2-3 weeks Buy Now Add To Cart
500mg 95% $716.00 2-3 weeks Buy Now Add To Cart
1g 95% $911.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,758.00 2-3 weeks Buy Now Add To Cart
5g 95% $2,587.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01A3KC
Chemical Name 3-[(2S)-1-[(tert-butoxy)carbonyl]pyrrolidin-2-yl]propanoic acid
CAS Number 65595-02-0
Molecular Formula C12H21NO4
Molecular Weight 243.2994
MDL Number MFCD11226805
SMILES OC(=O)CC[C@@H]1CCCN1C(=O)OC(C)(C)C

(2S)-1-[(1,1-Dimethylethoxy)carbonyl]-2-pyrrolidinepropanoic acid is a valuable compound widely utilized in chemical synthesis for its unique properties and versatile applications. As a chiral building block, this compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its stereochemistry and functional groups make it a key intermediate in the synthesis of complex molecules with high enantiomeric purity.In organic synthesis, (2S)-1-[(1,1-Dimethylethoxy)carbonyl]-2-pyrrolidinepropanoic acid serves as a precursor for the preparation of peptide-based drugs and amino acid derivatives. Its ability to serve as a protecting group for amines and carboxylic acids enhances its utility in peptide synthesis strategies, such as solid-phase peptide synthesis and solution-phase peptide coupling reactions. Moreover, its chiral nature enables the straightforward incorporation of stereochemical elements into organic molecules, making it indispensable in the development of novel therapeutic agents and chemical intermediates.Furthermore, the (2S)-1-[(1,1-Dimethylethoxy)carbonyl]-2-pyrrolidinepropanoic acid's compatibility with a wide range of coupling methods, including amidation and esterification reactions, allows for efficient and selective functional group transformations in organic synthesis. Its stability under various reaction conditions and compatibility with common reagents make it a preferred choice for chemists seeking to introduce structural diversity and complexity into their target molecules.Overall, (2S)-1-[(1,1-Dimethylethoxy)carbonyl]-2-pyrrolidinepropanoic acid stands out as a versatile and valuable building block in chemical synthesis, facilitating the construction of intricate molecular architectures with precision and efficiency. Its applications span across diverse areas of chemical research and development, making it an indispensable tool for synthetic chemists aiming to access novel compounds with therapeutic, agricultural, or materials science significance.
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