2-Chloro-6-hydroxypyridine-4-carbonitrile

95%

Reagent Code: #131282
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CAS Number 1556812-05-5

science Other reagents with same CAS 1556812-05-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.55 g/mol
Formula C₆H₃ClN₂O
badge Registry Numbers
MDL Number MFCD24366675
thermostat Physical Properties
Boiling Point 293.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.45±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its reactive functional groups. The compound's structure allows for easy modification, making it valuable in medicinal chemistry for constructing pyridine-based drug candidates. Also employed in research for developing new bioactive molecules with potential antimicrobial or anti-inflammatory properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,190.00
inventory 250mg
10-20 days ฿22,420.00

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2-Chloro-6-hydroxypyridine-4-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its reactive functional groups. The compound's structure allows for easy modification, making it valuable in medicinal chemistry for constructing pyridine-based drug candidates. Also employed in research for developing new bioactive molecules with potential antimicrobia

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for creating herbicides and insecticides due to its reactive functional groups. The compound's structure allows for easy modification, making it valuable in medicinal chemistry for constructing pyridine-based drug candidates. Also employed in research for developing new bioactive molecules with potential antimicrobial or anti-inflammatory properties.

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