2,6-Dichloro-5-fluoronicotinamide

98%

Reagent Code: #171517
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CAS Number 113237-20-0

science Other reagents with same CAS 113237-20-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.01 g/mol
Formula C₆H₃Cl₂FN₂O
thermostat Physical Properties
Melting Point 160-162°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of systemic insecticides targeting sucking pests. Its structure enables effective penetration into plant tissues, making it valuable in crop protection formulations. Also explored in pharmaceutical research for its potential bioactivity in heterocyclic compound development. Commonly employed in the creation of neonicotinoid analogs due to its halogenated pyridine backbone, enhancing binding affinity to insect nicotinic acetylcholine receptors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿150.00
5g
10-20 days ฿350.00
25g
10-20 days ฿1,090.00
100g
10-20 days ฿4,010.00
500g
10-20 days ฿20,010.00
2,6-Dichloro-5-fluoronicotinamide
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of systemic insecticides targeting sucking pests. Its structure enables effective penetration into plant tissues, making it valuable in crop protection formulations. Also explored in pharmaceutical research for its potential bioactivity in heterocyclic compound development. Commonly employed in the creation of neonicotinoid analogs due to its halogenated pyridine backbone, enhancing binding affinity to insect nic

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of systemic insecticides targeting sucking pests. Its structure enables effective penetration into plant tissues, making it valuable in crop protection formulations. Also explored in pharmaceutical research for its potential bioactivity in heterocyclic compound development. Commonly employed in the creation of neonicotinoid analogs due to its halogenated pyridine backbone, enhancing binding affinity to insect nicotinic acetylcholine receptors.

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