2-Chloro-5-methoxypyridine

98%

Reagent Code: #160034
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CAS Number 139585-48-1

science Other reagents with same CAS 139585-48-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.57 g/mol
Formula C₆H₆ClNO
thermostat Physical Properties
Boiling Point 213.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. It serves as a building block in the development of nicotinic acetylcholine receptor agonists used in crop protection. Also employed in the manufacture of certain antiviral and anti-inflammatory compounds due to its ability to enhance bioavailability and binding affinity in active molecules. Its chloro and methoxy functional groups allow for selective modifications in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,320.00
inventory 25g
10-20 days ฿13,540.00
inventory 100g
10-20 days ฿53,890.00

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2-Chloro-5-methoxypyridine
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. It serves as a building block in the development of nicotinic acetylcholine receptor agonists used in crop protection. Also employed in the manufacture of certain antiviral and anti-inflammatory compounds due to its ability to enhance bioavailability and binding affinity in active molecules. Its chloro and methoxy functional groups allow for selective mo

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and plant growth regulators. It serves as a building block in the development of nicotinic acetylcholine receptor agonists used in crop protection. Also employed in the manufacture of certain antiviral and anti-inflammatory compounds due to its ability to enhance bioavailability and binding affinity in active molecules. Its chloro and methoxy functional groups allow for selective modifications in multi-step organic syntheses.

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