(R)-2-(5-Chloropyridin-2-yl)-4-isopropyl-4,5-dihydrooxazole

97%, 99% e.e.

Reagent Code: #229239
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CAS Number 2757083-23-9

science Other reagents with same CAS 2757083-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.69 g/mol
Formula C₁₁H₁₃ClN₂O
thermostat Physical Properties
Boiling Point 323.9±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of agrochemicals, particularly in the production of neonicotinoid insecticides targeting the insect nervous system. Its chiral structure enables effective stereocontrol during asymmetric synthesis, enhancing the efficacy and selectivity of the final active ingredients against pests like chewing and sucking insects. The compound’s stability under various reaction conditions makes it suitable for multi-step industrial processes. It is also explored in the development of novel pesticides that bind to nicotinic acetylcholine receptors in insects, causing paralysis and death, with minimal impact on non-target species.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,060.00
inventory 250mg
10-20 days ฿20,580.00

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(R)-2-(5-Chloropyridin-2-yl)-4-isopropyl-4,5-dihydrooxazole
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Used as a key chiral intermediate in the synthesis of agrochemicals, particularly in the production of neonicotinoid insecticides targeting the insect nervous system. Its chiral structure enables effective stereocontrol during asymmetric synthesis, enhancing the efficacy and selectivity of the final active ingredients against pests like chewing and sucking insects. The compound’s stability under various reaction conditions makes it suitable for multi-step industrial processes. It is also explored in the

Used as a key chiral intermediate in the synthesis of agrochemicals, particularly in the production of neonicotinoid insecticides targeting the insect nervous system. Its chiral structure enables effective stereocontrol during asymmetric synthesis, enhancing the efficacy and selectivity of the final active ingredients against pests like chewing and sucking insects. The compound’s stability under various reaction conditions makes it suitable for multi-step industrial processes. It is also explored in the development of novel pesticides that bind to nicotinic acetylcholine receptors in insects, causing paralysis and death, with minimal impact on non-target species.

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