2-Chloro-3-fluoropyridine-4-carbaldehyde

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Reagent Code: #163899
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CAS Number 329794-28-7

science Other reagents with same CAS 329794-28-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.55 g/mol
Formula C₆H₃ClFNO
badge Registry Numbers
MDL Number MFCD04972388
thermostat Physical Properties
Boiling Point 231.7 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.424 g/mL at 25 °C
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating herbicides and plant growth regulators. It is also employed in the preparation of pyridine-based compounds with potential antimicrobial and antifungal properties. Due to the presence of reactive halogen groups and an aldehyde functionality, it serves as a versatile building block in cross-coupling reactions and heterocyclic chemistry for drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿580.00
5g
10-20 days ฿2,290.00
100g
10-20 days ฿26,600.00
25g
10-20 days ฿7,680.00

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2-Chloro-3-fluoropyridine-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating herbicides and plant growth regulators. It is also employed in the preparation of pyridine-based compounds with potential antimicrobial and antifungal properties. Due to the presence of reactive halogen groups and an aldehyde functionality, it serves as a versatile building block in cr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure allows for selective functionalization, making it valuable in creating herbicides and plant growth regulators. It is also employed in the preparation of pyridine-based compounds with potential antimicrobial and antifungal properties. Due to the presence of reactive halogen groups and an aldehyde functionality, it serves as a versatile building block in cross-coupling reactions and heterocyclic chemistry for drug discovery.

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