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503552-68-9

1-Pyrrolidinecarboxylicacid,3,4-diamino-,1,1-dimethylethylester,(3R,4R)-(9CI)

Catalog#: AR00E8GY  |   CAS#: 503552-68-9  |   MDL#: MFCD14635702  |   MF: C9H19N3O2  |   MW: 201.2661

Packsize Purity Price Availability Quantity
100mg 97% $120.00 Global Stock Buy Now Add To Cart
250mg 97% $200.00 Global Stock Buy Now Add To Cart
500mg 97% $333.00 Global Stock Buy Now Add To Cart
1g 97% $498.00 Global Stock Buy Now Add To Cart
5g 97% $1,496.00 Global Stock Buy Now Add To Cart
10g 97% $2,304.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00E8GY
Chemical Name 1-Pyrrolidinecarboxylicacid,3,4-diamino-,1,1-dimethylethylester,(3R,4R)-(9CI)
CAS Number 503552-68-9
Molecular Formula C9H19N3O2
Molecular Weight 201.2661
MDL Number MFCD14635702
SMILES N[C@@H]1CN(C[C@H]1N)C(=O)OC(C)(C)C

The compound (3R,4R)-tert-Butyl 3,4-diaminopyrrolidine-1-carboxylate is a versatile molecule used in chemical synthesis for the construction of complex organic compounds. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, (3R,4R)-tert-Butyl 3,4-diaminopyrrolidine-1-carboxylate can be utilized as a chiral ligand for transition metal-catalyzed reactions, enabling the selective formation of enantiomerically pure products. Its rigid structure and stereochemistry play a crucial role in directing the stereochemical outcome of the reactions, making it an essential tool for asymmetric synthesis.Furthermore, this compound can act as a protecting group for amines in organic synthesis. By temporarily masking the amino functionality, (3R,4R)-tert-Butyl 3,4-diaminopyrrolidine-1-carboxylate enables selective transformations at other reactive sites in a molecule, facilitating the synthesis of complex molecular architectures with improved control over regio- and stereochemistry.Overall, the strategic incorporation of (3R,4R)-tert-Butyl 3,4-diaminopyrrolidine-1-carboxylate in chemical synthesis enables chemists to efficiently access structurally diverse and stereochemically complex compounds, making it a valuable reagent in the field of organic chemistry.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H332-H335
Precautionary Statements P280-P305+P351+P338-P310
Class -
Packing Group -

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