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718611-17-7

(S)-Boc-3-Amino-3-phenylpropan-1-ol

Catalog#: AR005G1L  |   CAS#: 718611-17-7  |   MDL#: MFCD09025325  |   MF: C14H21NO3  |   MW: 251.3214

Packsize Purity Price Availability Quantity
1g 98% $41.00 Global Stock Buy Now Add To Cart
5g 98% $124.00 Global Stock Buy Now Add To Cart
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Catalog Number AR005G1L
Chemical Name (S)-Boc-3-Amino-3-phenylpropan-1-ol
CAS Number 718611-17-7
Molecular Formula C14H21NO3
Molecular Weight 251.3214
MDL Number MFCD09025325
SMILES OCC[C@@H](c1ccccc1)NC(=O)OC(C)(C)C

The (S)-Boc-3-Amino-3-phenylpropan-1-ol, also known as (S)-Boc-β-amino alcohol, serves as a valuable intermediate in chemical synthesis. This compound is commonly utilized as a chiral building block due to its specific stereochemistry and functional groups. One of the key applications of (S)-Boc-3-Amino-3-phenylpropan-1-ol is in the synthesis of pharmaceuticals and agrochemicals.In organic synthesis, (S)-Boc-3-Amino-3-phenylpropan-1-ol can be used as a precursor for the creation of various chiral molecules with defined stereochemistry. Its Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at specific sites, enabling control over the overall stereochemical outcome of the synthetic pathway. This compound can participate in reactions such as acylation, alkylation, and cross-coupling to introduce different functional groups and expand the molecular diversity of the final product.Furthermore, (S)-Boc-3-Amino-3-phenylpropan-1-ol can be employed in asymmetric synthesis to access enantiomerically pure compounds. By utilizing this chiral building block, chemists can efficiently construct molecules with high optical purity, which is crucial for the development of advanced pharmaceuticals and biologically active compounds. Its versatile reactivity and stereochemical attributes make it a valuable tool in the hands of synthetic chemists aiming to create complex and structurally diverse molecules for various applications.
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