5-Chloro-2-hydroxy-6-methylnicotinonitrile

95%

Reagent Code: #163789
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CAS Number 1163297-82-2

science Other reagents with same CAS 1163297-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.58 g/mol
Formula C₇H₅ClN₂O
badge Registry Numbers
MDL Number MFCD22689336
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor modulators and anti-inflammatory agents. It serves in agrochemical formulations for developing herbicides and plant growth regulators due to its reactive nitrile and hydroxyl groups. The compound is also employed in research for heterocyclic compound development, enabling the construction of complex nitrogen-containing rings found in bioactive molecules. Its chloro functionality allows for selective substitutions, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,960.00
inventory 250mg
10-20 days ฿3,310.00
inventory 1g
10-20 days ฿8,890.00
inventory 5g
10-20 days ฿30,190.00
inventory 10g
10-20 days ฿52,490.00

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5-Chloro-2-hydroxy-6-methylnicotinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor modulators and anti-inflammatory agents. It serves in agrochemical formulations for developing herbicides and plant growth regulators due to its reactive nitrile and hydroxyl groups. The compound is also employed in research for heterocyclic compound development, enabling the construction of complex nitrogen-containing rings found in bioactive molecules. Its chloro functionality allows for

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor modulators and anti-inflammatory agents. It serves in agrochemical formulations for developing herbicides and plant growth regulators due to its reactive nitrile and hydroxyl groups. The compound is also employed in research for heterocyclic compound development, enabling the construction of complex nitrogen-containing rings found in bioactive molecules. Its chloro functionality allows for selective substitutions, making it valuable in medicinal chemistry for structure-activity relationship studies.

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