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939793-16-5

tert-Butyl 3-bromopyrrolidine-1-carboxylate

Catalog#: AR005XGE  |   CAS#: 939793-16-5  |   MDL#: MFCD08752478  |   MF: C9H16BrNO2  |   MW: 250.1328

Packsize Purity Price Availability Quantity
100mg 97% $2.00 Global Stock Buy Now Add To Cart
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $9.00 Global Stock Buy Now Add To Cart
5g 97% $32.00 Global Stock Buy Now Add To Cart
10g 97% $52.00 Global Stock Buy Now Add To Cart
25g 97% $113.00 Global Stock Buy Now Add To Cart
100g 97% $416.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005XGE
Chemical Name tert-Butyl 3-bromopyrrolidine-1-carboxylate
CAS Number 939793-16-5
Molecular Formula C9H16BrNO2
Molecular Weight 250.1328
MDL Number MFCD08752478
SMILES BrC1CCN(C1)C(=O)OC(C)(C)C

1-Boc-3-bromopyrrolidine is a versatile compound widely used in chemical synthesis for its unique reactivity and structural properties. Thanks to its Boc (tert-butoxycarbonyl) protecting group, this compound is particularly valuable in organic reactions that require selective manipulation of amine functionalities. The 3-bromopyrrolidine moiety adds additional complexity and diversity to the molecule, enabling it to participate in a variety of synthetic transformations.In organic synthesis, 1-Boc-3-bromopyrrolidine serves as a key building block for the preparation of various complex molecules, such as pharmaceutical intermediates, agrochemicals, and materials. Its reactivity can be harnessed for the construction of biologically active compounds and the modification of existing chemical entities. The presence of the Boc protecting group allows for controlled deprotection under mild conditions, making it a valuable tool in the synthesis of sensitive molecules.Additionally, the 3-bromopyrrolidine functionality can undergo diverse transformations, including nucleophilic substitution, palladium-catalyzed cross-coupling reactions, and cycloaddition reactions, expanding the synthetic possibilities of 1-Boc-3-bromopyrrolidine. Its versatile nature and compatibility with a wide range of reaction conditions make it a valuable asset in the toolkit of synthetic chemists seeking to access complex molecules efficiently and selectively.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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