tert-Butyl (1-(6-ethoxy-2-(methylthio)pyrimidin-4-yl)piperidin-4-yl)carbamate

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Reagent Code: #151249
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CAS Number 1353978-27-4

science Other reagents with same CAS 1353978-27-4

blur_circular Chemical Specifications

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Weight 368.49 g/mol
Formula C₁₇H₂₈N₄O₃S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme targets involved in cellular signaling pathways, making it valuable in drug discovery for cancer and inflammatory diseases. The tert-butyl carbamate group acts as a protecting group during peptide or peptidomimetic synthesis, allowing selective reaction at other functional sites. It is also employed in the preparation of bioactive molecules where the piperidine and pyrimidine moieties contribute to target selectivity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,690.00
inventory 250mg
10-20 days ฿13,730.00
inventory 1g
10-20 days ฿43,220.00

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tert-Butyl (1-(6-ethoxy-2-(methylthio)pyrimidin-4-yl)piperidin-4-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme targets involved in cellular signaling pathways, making it valuable in drug discovery for cancer and inflammatory diseases. The tert-butyl carbamate group acts as a protecting group during peptide or peptidomimetic synthesis, allowing selective reaction at other functional sites. It is also employed in the preparation of bioactive mo

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors. Its structure supports binding to specific enzyme targets involved in cellular signaling pathways, making it valuable in drug discovery for cancer and inflammatory diseases. The tert-butyl carbamate group acts as a protecting group during peptide or peptidomimetic synthesis, allowing selective reaction at other functional sites. It is also employed in the preparation of bioactive molecules where the piperidine and pyrimidine moieties contribute to target selectivity and metabolic stability.

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