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550378-07-9

tert-butyl (2R)-2-(2-aminoethyl)pyrrolidine-1-carboxylate

Catalog#: AR00D9TE  |   CAS#: 550378-07-9  |   MDL#: MFCD04115290  |   MF: C11H22N2O2  |   MW: 214.3046

Packsize Purity Price Availability Quantity
100mg 97% $60.00 Global Stock Buy Now Add To Cart
250mg 97% $100.00 Global Stock Buy Now Add To Cart
500mg 97% $166.00 Global Stock Buy Now Add To Cart
1g 97% $255.00 Global Stock Buy Now Add To Cart
5g 97% $753.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00D9TE
Chemical Name tert-butyl (2R)-2-(2-aminoethyl)pyrrolidine-1-carboxylate
CAS Number 550378-07-9
Molecular Formula C11H22N2O2
Molecular Weight 214.3046
MDL Number MFCD04115290
SMILES NCC[C@H]1CCCN1C(=O)OC(C)(C)C

$Name$ is a multifunctional compound widely utilized in chemical synthesis. Specifically, (R)-1-Boc-2-(Aminoethyl)pyrrolidine plays a crucial role as a key building block in the creation of various complex organic molecules. With its unique structure and reactivity, this compound serves as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, (R)-1-Boc-2-(Aminoethyl)pyrrolidine is commonly employed as a chiral amine, enabling the incorporation of asymmetry into molecular structures. Its Boc (tert-butoxycarbonyl) protected amine group offers strategic opportunities for selective functionalization and controlled reactivity in organic reactions. This compound is particularly valuable in the preparation of enantiopure compounds, where chirality plays a critical role in determining biological activity and properties.Furthermore, (R)-1-Boc-2-(Aminoethyl)pyrrolidine serves as a crucial component in the construction of peptidomimetics and bioactive molecules. By virtue of its pyrrolidine core and aminoethyl side chain, this compound can participate in diverse synthetic transformations such as ring-closing reactions, cross-coupling reactions, and asymmetric catalysis. Its presence in the molecular framework imparts specific functionalities that are essential for molecular recognition and bioactivity.Overall, the application of (R)-1-Boc-2-(Aminoethyl)pyrrolidine in chemical synthesis underscores its significance as a versatile building block with unique structural features and reactivity. Its strategic incorporation into synthetic pathways enhances the efficiency and diversity of molecule construction, facilitating the development of novel compounds with potential applications in various fields.
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GHS Pictogram
Signal Word Danger
UN# 2735
Hazard Statements H314-H318
Precautionary Statements P280-P305+P351+P338-P310
Class 8
Packing Group

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