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1312798-50-7

1-Piperidinecarboxylic acid, 3-amino-4-hydroxy-, 1,1-dimethylethyl ester, (3R,4S)-

Catalog#: AR000WJS  |   CAS#: 1312798-50-7  |   MDL#: MFCD28502771  |   MF: C10H20N2O3  |   MW: 216.2774

Packsize Purity Price Availability Quantity
50mg 97% $78.00 Global Stock Buy Now Add To Cart
100mg 97% $87.00 Global Stock Buy Now Add To Cart
250mg 97% $139.00 Global Stock Buy Now Add To Cart
500mg 97% $174.00 Global Stock Buy Now Add To Cart
1g 97% $295.00 Global Stock Buy Now Add To Cart
5g 97% $1,247.00 Global Stock Buy Now Add To Cart
10g 97% $2,164.00 Global Stock Buy Now Add To Cart
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Catalog Number AR000WJS
Chemical Name 1-Piperidinecarboxylic acid, 3-amino-4-hydroxy-, 1,1-dimethylethyl ester, (3R,4S)-
CAS Number 1312798-50-7
Molecular Formula C10H20N2O3
Molecular Weight 216.2774
MDL Number MFCD28502771
SMILES O[C@H]1CCN(C[C@H]1N)C(=O)OC(C)(C)C

$xname$ is a versatile compound that plays a crucial role in various chemical synthesis reactions. This compound, often referred to as tert-butyl (3R,4S)-3-amino-4-hydroxypiperidine-1-carboxylate, is highly valued for its ability to serve as a key building block in the production of complex organic molecules. It is particularly valued in the pharmaceutical industry, where it is used in the synthesis of important drug candidates and intermediates.In chemical synthesis, $xname$ acts as a chiral amino acid derivative, providing a structurally unique scaffold for the creation of diverse compounds. Its stereochemistry, with the specified R and S configurations, enables precise control over the spatial orientation of functional groups in the target molecules. This allows chemists to tailor the properties and interactions of the final products, making $xname$ a valuable tool for designing new pharmaceuticals, agrochemicals, and other specialty chemicals.Furthermore, the tert-butyl group in $xname$ confers steric hindrance and increased stability to the molecule, making it particularly useful in reactions that require selective transformations or protection of specific functional groups. By strategically manipulating the functional groups of $xname$, chemists can generate a wide range of derivatives with varied properties and reactivities, opening up possibilities for innovative synthetic pathways and the discovery of novel compounds.Overall, the application of tert-butyl (3R,4S)-3-amino-4-hydroxypiperidine-1-carboxylate in chemical synthesis is instrumental in pushing the boundaries of organic chemistry and drug discovery. Its unique structural features and versatility make it an invaluable asset for researchers working to develop cutting-edge technologies and novel compounds with diverse applications.
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