tert-Butyl (4-(3-(dimethoxyphosphoryl)-2-oxopropyl)phenyl)carbamate

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Reagent Code: #153375
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CAS Number 494224-44-1

science Other reagents with same CAS 494224-44-1

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inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in pharmaceutical synthesis as a protected intermediate, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides amine protection during peptide or heterocycle assembly, while the dimethoxyphosphoryl moiety allows for further functionalization via Horner-Wadsworth-Emmons olefination or phosphorylation reactions. Its structure supports the construction of complex drug candidates requiring selective reactivity and stability under multi-step synthesis conditions. Commonly employed in medicinal chemistry for optimizing metabolic stability and target binding affinity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿14,650.00
inventory 50mg
10-20 days ฿26,380.00
inventory 100mg
10-20 days ฿49,410.00

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tert-Butyl (4-(3-(dimethoxyphosphoryl)-2-oxopropyl)phenyl)carbamate
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Used in pharmaceutical synthesis as a protected intermediate, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides amine protection during peptide or heterocycle assembly, while the dimethoxyphosphoryl moiety allows for further functionalization via Horner-Wadsworth-Emmons olefination or phosphorylation reactions. Its structure supports the construction of complex drug candidates requiring selective reactivity and stability unde

Used in pharmaceutical synthesis as a protected intermediate, particularly in the development of kinase inhibitors and other bioactive molecules. The tert-butyl carbamate (Boc) group provides amine protection during peptide or heterocycle assembly, while the dimethoxyphosphoryl moiety allows for further functionalization via Horner-Wadsworth-Emmons olefination or phosphorylation reactions. Its structure supports the construction of complex drug candidates requiring selective reactivity and stability under multi-step synthesis conditions. Commonly employed in medicinal chemistry for optimizing metabolic stability and target binding affinity.

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