TRANS-(4-AMINO-TETRAHYDRO-PYRAN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER

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Reagent Code: #244895
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CAS Number 1316830-74-6

science Other reagents with same CAS 1316830-74-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD28053712
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drug design for improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing peptidomimetics and proline analogs, aiding in the optimization of pharmacokinetic properties. Also utilized in solid-phase and solution-phase peptide synthesis due to the presence of protected amine functionality, allowing selective deprotection and coupling reactions.

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inventory 100mg
10-20 days ฿14,730.00

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TRANS-(4-AMINO-TETRAHYDRO-PYRAN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drug design for improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing peptidomimetics and proline analogs, aiding in the optimization of pharmacokinetic properties. Also utilized in solid-phase and solution
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drug design for improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing peptidomimetics and proline analogs, aiding in the optimization of pharmacokinetic properties. Also utilized in solid-phase and solution-phase peptide synthesis due to the presence of protected amine functionality, allowing selective deprotection and coupling reactions.
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