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569660-97-5

(R)-tert-Butyl 3-bromopyrrolidine-1-carboxylate

Catalog#: AR00EDVJ  |   CAS#: 569660-97-5  |   MDL#: MFCD17214727  |   MF: C9H16BrNO2  |   MW: 250.1328

Packsize Purity Price Availability Quantity
100mg 97% $14.00 Global Stock Buy Now Add To Cart
250mg 97% $29.00 Global Stock Buy Now Add To Cart
1g 97% $83.00 Global Stock Buy Now Add To Cart
5g 97% $319.00 Global Stock Buy Now Add To Cart
10g 97% $638.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EDVJ
Chemical Name (R)-tert-Butyl 3-bromopyrrolidine-1-carboxylate
CAS Number 569660-97-5
Molecular Formula C9H16BrNO2
Molecular Weight 250.1328
MDL Number MFCD17214727
SMILES Br[C@@H]1CCN(C1)C(=O)OC(C)(C)C

(R)-1-Boc-3-bromopyrrolidine is a versatile compound commonly used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable intermediate in organic synthesis.One of the important applications of (R)-1-Boc-3-bromopyrrolidine is in the synthesis of chiral compounds. The presence of the Boc (tert-butoxycarbonyl) protecting group on the nitrogen atom provides stability and allows for selective functionalization of the pyrrolidine ring. This compound can be used as a chiral auxiliary in asymmetric synthesis or as a precursor for the preparation of chiral ligands and catalysts.Furthermore, the bromo group on the pyrrolidine ring can serve as a useful handle for further derivatization through various cross-coupling reactions such as Suzuki-Miyaura, Heck, or Sonogashira reactions. This enables chemists to introduce different functional groups or substituents at the bromo position, thereby expanding the molecular diversity and potential applications of the compound.Overall, (R)-1-Boc-3-bromopyrrolidine plays a crucial role in the synthesis of complex organic molecules with defined stereochemistry, making it a valuable tool for medicinal chemists and chemical researchers in the development of new compounds with potential biological activity and therapeutic applications.
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