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Home  > 1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-(methoxymethyl)-, 1,1-dimethylethyl ester, (2R,4R)-

BA07374

1146951-37-2 | 1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-(methoxymethyl)-, 1,1-dimethylethyl ester, (2R,4R)-

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $232.00 $162.00 -   +
1g 95% in stock $569.00 $398.00 -   +

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

*All prices are in USD.

Description
Catalog Number: BA07374
Chemical Name: 1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-(methoxymethyl)-, 1,1-dimethylethyl ester, (2R,4R)-
CAS Number: 1146951-37-2
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887
MDL Number: MFCD31635832
SMILES: COC[C@H]1C[C@H](CN1C(=O)OC(C)(C)C)O

 

Upstream Synthesis Route
  • 1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-(methoxymethyl)-, 1,1-dimethylethyl ester, (2R,4R)- is a valuable compound used in chemical synthesis for its versatile reactivity and stereochemical properties. This compound is commonly employed as a chiral building block in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.One notable application of this compound is in the synthesis of chiral intermediates for the pharmaceutical industry. Its 2R,4R stereochemistry imparts specific molecular properties that are crucial for the efficacy and selectivity of the final drug products. By incorporating this compound into the synthesis of drug molecules, chemists can control the stereochemical outcome of reactions, leading to enhanced biological activity and reduced side effects.Additionally, 1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-(methoxymethyl)-, 1,1-dimethylethyl ester, (2R,4R)- can serve as a key starting material for the construction of complex natural products and bioactive compounds. Its unique structural features enable the formation of diverse chemical bonds and functional groups, allowing for the efficient assembly of intricate molecular architectures.Overall, this compound plays a crucial role in chemical synthesis by enabling the creation of stereochemically pure and structurally complex molecules with potential applications in various industries, highlighting its significance in modern organic chemistry practices.
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