2-Chloro-3-fluoro-4-nitropyridine

97%

Reagent Code: #160676
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CAS Number 109613-90-3

science Other reagents with same CAS 109613-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.53 g/mol
Formula C₅H₂ClFN₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with antimicrobial and anti-inflammatory properties. Its structure, featuring chloro, fluoro, and nitro groups, allows for selective substitutions, enhancing cell permeability, target specificity, and conversion to amino groups, making it valuable in constructing pyridine-based drug candidates. The nitro group can be readily reduced to an amino group, a key step in API synthesis. Also employed in agrochemical manufacturing for creating herbicides and fungicides due to its reactivity and stability under various reaction conditions. Commonly utilized in research laboratories for developing novel heterocyclic compounds in medicinal chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿850.00
250mg
10-20 days ฿1,640.00
500mg
10-20 days ฿2,880.00
1g
10-20 days ฿5,330.00
5g
10-20 days ฿21,330.00
10g
10-20 days ฿36,000.00
25g
10-20 days ฿72,000.00
2-Chloro-3-fluoro-4-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with antimicrobial and anti-inflammatory properties. Its structure, featuring chloro, fluoro, and nitro groups, allows for selective substitutions, enhancing cell permeability, target specificity, and conversion to amino groups, making it valuable in constructing pyridine-based drug candidates. The nitro group can be readily reduced to an amino group, a key step in API

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with antimicrobial and anti-inflammatory properties. Its structure, featuring chloro, fluoro, and nitro groups, allows for selective substitutions, enhancing cell permeability, target specificity, and conversion to amino groups, making it valuable in constructing pyridine-based drug candidates. The nitro group can be readily reduced to an amino group, a key step in API synthesis. Also employed in agrochemical manufacturing for creating herbicides and fungicides due to its reactivity and stability under various reaction conditions. Commonly utilized in research laboratories for developing novel heterocyclic compounds in medicinal chemistry.

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