4-Chloro-5,6-difluoronicotinic acid

95%

Reagent Code: #160174
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CAS Number 851386-32-8

science Other reagents with same CAS 851386-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.54 g/mol
Formula C₆H₂ClF₂NO₂
badge Registry Numbers
MDL Number MFCD09031172
thermostat Physical Properties
Melting Point 117-118°C
Boiling Point 297.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. Its halogen substitution pattern enables selective reactivity, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the nicotinic core into bioactive molecules. Also utilized in the preparation of kinase inhibitors and other medicinal agents where fluorine substitution enhances metabolic stability and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,540.00
inventory 250mg
10-20 days ฿2,480.00
inventory 500mg
10-20 days ฿4,610.00
inventory 1g
10-20 days ฿7,680.00
inventory 5g
10-20 days ฿34,500.00
inventory 10g
10-20 days ฿64,930.00
inventory 25g
10-20 days ฿161,590.00

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4-Chloro-5,6-difluoronicotinic acid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. Its halogen substitution pattern enables selective reactivity, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the nicotinic core into bioactive molecules. Also utilized in the preparation of kinase inhibitors and other medicinal agents where fluorine substitution

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. Its halogen substitution pattern enables selective reactivity, making it valuable in constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the nicotinic core into bioactive molecules. Also utilized in the preparation of kinase inhibitors and other medicinal agents where fluorine substitution enhances metabolic stability and binding affinity.

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