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Home  > tert-Butyl (3r,4r)-3-amino-4-(hydroxymethyl)pyrrolidine-1-carboxylate

AE24665

1207853-71-1 | tert-Butyl (3r,4r)-3-amino-4-(hydroxymethyl)pyrrolidine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $185.00 $129.00 -   +
250mg 98% in stock $346.00 $242.00 -   +
1g 98% in stock $1,039.00 $727.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE24665
Chemical Name: tert-Butyl (3r,4r)-3-amino-4-(hydroxymethyl)pyrrolidine-1-carboxylate
CAS Number: 1207853-71-1
Molecular Formula: C10H20N2O3
Molecular Weight: 216.2774
MDL Number: MFCD12031285
SMILES: OC[C@@H]1CN(C[C@@H]1N)C(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • The compound (3R,4R)-tert-Butyl 3-amino-4-(hydroxymethyl)pyrrolidine-1-carboxylate is a valuable reagent in chemical synthesis due to its unique structural features and versatile reactivity. Its chiral nature, characterized by the 3R and 4R stereochemistry, makes it a valuable building block for asymmetric synthesis.In organic chemistry, this compound can serve as a key intermediate in the synthesis of various pharmaceuticals, natural products, and chiral ligands. Its amino and hydroxymethyl groups offer functional handles for further modification, allowing for the creation of complex molecular structures with high stereochemical control.One of the notable applications of (3R,4R)-tert-Butyl 3-amino-4-(hydroxymethyl)pyrrolidine-1-carboxylate is in the preparation of enantiomerically pure compounds, which are crucial in drug discovery and development. By utilizing this compound as a starting material, chemists can access enantioenriched molecules that exhibit specific biological activities and improved pharmacological properties.Furthermore, the presence of a tert-butyl group in the structure enhances the compound's stability and facilitates its manipulation in various synthetic transformations. Overall, (3R,4R)-tert-Butyl 3-amino-4-(hydroxymethyl)pyrrolidine-1-carboxylate offers chemists a powerful tool for designing and constructing complex molecules with high levels of stereochemical control.
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