tert-Butyl 6-chloronicotinate

≥95%

Reagent Code: #148426
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CAS Number 115309-57-4

science Other reagents with same CAS 115309-57-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.66 g/mol
Formula C₁₀H₁₂ClNO₂
badge Registry Numbers
MDL Number MFCD08277247
thermostat Physical Properties
Boiling Point 270.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in medicinal chemistry for constructing pyridine-based drug candidates. Commonly employed in the preparation of kinase inhibitors and agrochemicals due to its reactive chloro and ester functionalities. Its tert-butyl ester group allows for selective deprotection under mild acidic conditions, enabling stepwise synthesis in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,080.00
inventory 5g
10-20 days ฿4,750.00
inventory 10g
10-20 days ฿9,470.00
inventory 25g
10-20 days ฿20,530.00

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tert-Butyl 6-chloronicotinate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in medicinal chemistry for constructing pyridine-based drug candidates. Commonly employed in the preparation of kinase inhibitors and agrochemicals due to its reactive chloro and ester functionalities. Its tert-butyl ester group allows for selective deprotection under mild acidic conditions, enabling stepwise s

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in medicinal chemistry for constructing pyridine-based drug candidates. Commonly employed in the preparation of kinase inhibitors and agrochemicals due to its reactive chloro and ester functionalities. Its tert-butyl ester group allows for selective deprotection under mild acidic conditions, enabling stepwise synthesis in complex molecule assembly.

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