2,6-Dichloro-3-hydroxyisonicotinic acid

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Reagent Code: #171327
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CAS Number 185422-96-2

science Other reagents with same CAS 185422-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208 g/mol
Formula C₆H₃Cl₂NO₃
badge Registry Numbers
MDL Number MFCD03411718
thermostat Physical Properties
Boiling Point 548.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antitubercular drugs. It plays an important role in the development of compounds targeting Mycobacterium tuberculosis due to its structural compatibility with biologically active molecules. Its functional groups allow for easy modification in multi-step organic syntheses, making it valuable in medicinal chemistry for building heterocyclic systems. Also utilized in research settings for designing enzyme inhibitors and probing structure-activity relationships in drug candidates.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,400.00
inventory 100mg
10-20 days ฿3,058.00
inventory 250mg
10-20 days ฿9,820.00
inventory 1g
10-20 days ฿24,640.00
inventory 5g
10-20 days ฿66,970.00

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2,6-Dichloro-3-hydroxyisonicotinic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antitubercular drugs. It plays an important role in the development of compounds targeting Mycobacterium tuberculosis due to its structural compatibility with biologically active molecules. Its functional groups allow for easy modification in multi-step organic syntheses, making it valuable in medicinal chemistry for building heterocyclic systems. Also utilized in research settings for designing enzym

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antitubercular drugs. It plays an important role in the development of compounds targeting Mycobacterium tuberculosis due to its structural compatibility with biologically active molecules. Its functional groups allow for easy modification in multi-step organic syntheses, making it valuable in medicinal chemistry for building heterocyclic systems. Also utilized in research settings for designing enzyme inhibitors and probing structure-activity relationships in drug candidates.

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