Ethyl 6-ethynylpicolinate

≥95%

Reagent Code: #183581
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CAS Number 1379302-65-4

science Other reagents with same CAS 1379302-65-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.18 g/mol
Formula C₁₀H₉NO₂
badge Registry Numbers
MDL Number MFCD20037583
thermostat Physical Properties
Boiling Point 302.8±27.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its alkyne functionality allows for efficient coupling reactions, such as Sonogashira cross-coupling, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in the preparation of pyridine-based derivatives with potential biological activity, including anti-inflammatory and antiviral agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿630.00
inventory 250mg
10-20 days ฿1,570.00
inventory 1g
10-20 days ฿5,680.00
inventory 5g
10-20 days ฿27,260.00

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Ethyl 6-ethynylpicolinate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its alkyne functionality allows for efficient coupling reactions, such as Sonogashira cross-coupling, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in the preparation of pyridine-based derivatives with potential biological

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its alkyne functionality allows for efficient coupling reactions, such as Sonogashira cross-coupling, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in the preparation of pyridine-based derivatives with potential biological activity, including anti-inflammatory and antiviral agents.

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