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615582-98-4

(2S,4R)-tert-butyl 4-((tert-butyldiphenylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylate

Catalog#: AR01DHB4  |   CAS#: 615582-98-4  |   MDL#: MFCD31706246  |   MF: C26H37NO4Si  |   MW: 455.6618

Packsize Purity Price Availability Quantity
100mg 97% $22.00 Global Stock Buy Now Add To Cart
250mg 97% $51.00 Global Stock Buy Now Add To Cart
1g 97% $193.00 Global Stock Buy Now Add To Cart
5g 97% $786.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01DHB4
Chemical Name (2S,4R)-tert-butyl 4-((tert-butyldiphenylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
CAS Number 615582-98-4
Molecular Formula C26H37NO4Si
Molecular Weight 455.6618
MDL Number MFCD31706246
SMILES OC[C@@H]1C[C@H](CN1C(=O)OC(C)(C)C)O[Si](C(C)(C)C)(c1ccccc1)c1ccccc1

The tert-Butyl (2S,4R)-4-((tert-butyldiphenylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylate is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it an essential building block in the creation of complex molecules and pharmaceuticals.In chemical synthesis, this compound serves as a protective group for hydroxyl and amine functional groups. By selectively blocking these reactive sites with the tert-butyldiphenylsilyl group, the compound allows for specific reactions to occur at other functional groups within the molecule. This controlled reactivity is crucial in the synthesis of intricate organic compounds where precise manipulations are required.Furthermore, the tert-Butyl (2S,4R)-4-((tert-butyldiphenylsilyl)oxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylate can also act as a chiral auxiliary, imparting stereochemical control in asymmetric synthesis. Its 2S,4R stereochemistry plays a key role in determining the spatial arrangement of atoms in the final product, ensuring the desired enantiomeric purity.Overall, this compound's role in chemical synthesis is indispensable for the construction of structurally complex molecules with high stereochemical precision and selectivity.
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