2-(2-Chloro-4-fluorophenoxy)aceticacid

98%

Reagent Code: #166532
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CAS Number 399-41-7

science Other reagents with same CAS 399-41-7

blur_circular Chemical Specifications

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Weight 204.59 g/mol
Formula C₈H₆ClFO₃
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MDL Number MFCD03422210
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Storage Room temperature

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Used primarily as an intermediate in the synthesis of phenoxy herbicides, particularly selective broadleaf herbicides. It plays a key role in agrochemical formulations targeting weeds in cereal crops, lawns, and turf without harming grass species. The compound's structure allows for effective plant growth regulation by mimicking natural auxins, leading to uncontrolled growth and eventual death of susceptible plants. It is also utilized in the production of ester and salt derivatives that enhance herbicidal activity and solubility. Due to its reactivity, it serves as a building block in organic synthesis for fluorinated and chlorinated aromatic compounds in crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,410.00
inventory 1g
10-20 days ฿9,410.00
inventory 5g
10-20 days ฿43,650.00
inventory 100mg
10-20 days ฿3,120.00

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2-(2-Chloro-4-fluorophenoxy)aceticacid
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Used primarily as an intermediate in the synthesis of phenoxy herbicides, particularly selective broadleaf herbicides. It plays a key role in agrochemical formulations targeting weeds in cereal crops, lawns, and turf without harming grass species. The compound's structure allows for effective plant growth regulation by mimicking natural auxins, leading to uncontrolled growth and eventual death of susceptible plants. It is also utilized in the production of ester and salt derivatives that enhance herbicid

Used primarily as an intermediate in the synthesis of phenoxy herbicides, particularly selective broadleaf herbicides. It plays a key role in agrochemical formulations targeting weeds in cereal crops, lawns, and turf without harming grass species. The compound's structure allows for effective plant growth regulation by mimicking natural auxins, leading to uncontrolled growth and eventual death of susceptible plants. It is also utilized in the production of ester and salt derivatives that enhance herbicidal activity and solubility. Due to its reactivity, it serves as a building block in organic synthesis for fluorinated and chlorinated aromatic compounds in crop protection chemistry.

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