Ethyl (R)-2-[4-[(6-Chloroquinoxalin-2-yl)oxy]phenoxy]propanoate

Analysis of the controls, 96%

Reagent Code: #228405
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Alias Jingqianhe Ling
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CAS Number 100646-51-3

science Other reagents with same CAS 100646-51-3

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Weight 372.8 g/mol
Formula C₁₉H₁₇ClN₂O₄
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MDL Number MFCD09028086
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Quizalofop-P-ethyl is a selective post-emergence herbicide belonging to the aryloxyphenoxypropionate class. It is used to control annual and perennial grass weeds in broadleaf crops such as soybeans, cotton, peanuts, and vegetables. The compound inhibits acetyl-CoA carboxylase (ACCase), an enzyme essential for fatty acid synthesis in grasses, leading to membrane disruption and plant death. Its (R)-enantiomer configuration enhances potency and selectivity, allowing safe use in dicotyledonous crops. Due to its chiral properties and biological activity, it has also been explored in pharmaceutical research for potential interactions with chiral-sensitive targets.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,890.00

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Ethyl (R)-2-[4-[(6-Chloroquinoxalin-2-yl)oxy]phenoxy]propanoate
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Quizalofop-P-ethyl is a selective post-emergence herbicide belonging to the aryloxyphenoxypropionate class. It is used to control annual and perennial grass weeds in broadleaf crops such as soybeans, cotton, peanuts, and vegetables. The compound inhibits acetyl-CoA carboxylase (ACCase), an enzyme essential for fatty acid synthesis in grasses, leading to membrane disruption and plant death. Its (R)-enantiomer configuration enhances potency and selectivity, allowing safe use in dicotyledonous crops. Due to

Quizalofop-P-ethyl is a selective post-emergence herbicide belonging to the aryloxyphenoxypropionate class. It is used to control annual and perennial grass weeds in broadleaf crops such as soybeans, cotton, peanuts, and vegetables. The compound inhibits acetyl-CoA carboxylase (ACCase), an enzyme essential for fatty acid synthesis in grasses, leading to membrane disruption and plant death. Its (R)-enantiomer configuration enhances potency and selectivity, allowing safe use in dicotyledonous crops. Due to its chiral properties and biological activity, it has also been explored in pharmaceutical research for potential interactions with chiral-sensitive targets.

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