tert-Butyl (6-(hydroxymethyl)pyridin-3-yl)carbamate

95%

Reagent Code: #148680
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CAS Number 323578-38-7

science Other reagents with same CAS 323578-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.26 g/mol
Formula C₁₁H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD12031249
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in medicinal chemistry research. The presence of both hydroxymethyl and carbamate functional groups enables coupling reactions and protection strategies during multi-step syntheses. Commonly employed in the preparation of pyridine-based derivatives with potential therapeutic activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,230.00
inventory 1g
10-20 days ฿23,110.00
inventory 5g
10-20 days ฿81,690.00

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tert-Butyl (6-(hydroxymethyl)pyridin-3-yl)carbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in medicinal chemistry research. The presence of both hydroxymethyl and carbamate functional groups enables coupling reactions and protection strategies during multi-step syntheses. Commonly employed in the preparation of pyridine-based derivatives with potentia

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure allows for selective modification in drug design, making it valuable in medicinal chemistry research. The presence of both hydroxymethyl and carbamate functional groups enables coupling reactions and protection strategies during multi-step syntheses. Commonly employed in the preparation of pyridine-based derivatives with potential therapeutic activity.

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