tert-Butyl (5-chloro-3-hydroxypyridin-2-yl)carbamate

97%

Reagent Code: #113346
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CAS Number 1609402-46-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.67 g/mol
Formula C₁₀H₁₃ClN₂O₃
badge Registry Numbers
MDL Number MFCD27935389
thermostat Physical Properties
Boiling Point 351.4±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and inflammatory disorders. Its structure is often incorporated into drug candidates that modulate specific enzymes or receptors, making it valuable for creating potential therapeutic agents. Additionally, it is used in organic synthesis to build complex molecules due to its reactive functional groups, which allow for further chemical modifications. Its application is also seen in the development of agrochemicals, where it contributes to the creation of compounds with pesticidal or herbicidal properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿7,515.00
inventory 1g
10-20 days ฿1,557.00
inventory 5g
10-20 days ฿4,698.00
tert-Butyl (5-chloro-3-hydroxypyridin-2-yl)carbamate
This chemical is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and inflammatory disorders. Its structure is often incorporated into drug candidates that modulate specific enzymes or receptors, making it valuable for creating potential therapeutic agents. Additionally, it is used in organic synthesis to build complex molecules due to its reactive functional groups, which allow for further chemical modifications. Its application is also seen in the development of agrochemicals, where it contributes to the creation of compounds with pesticidal or herbicidal properties.
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