N-(4-(tert-Butyl)phenyl)-2-chloroacetamide

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Reagent Code: #215514
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CAS Number 20330-46-5

science Other reagents with same CAS 20330-46-5

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Weight 225.71 g/mol
Formula C₁₂H₁₆ClNO
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MDL Number MFCD00084910
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure, featuring the tert-butyl and chloroacetamide groups, supports the creation of compounds with biological activity in crop protection, enhancing stability and target specificity. Also employed in research settings for the preparation of specialty organic molecules requiring selective reactivity. The chloroacetamide group enables alkylation reactions, making it valuable in building complex molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,320.00
inventory 250mg
10-20 days ฿4,770.00
inventory 1g
10-20 days ฿9,690.00

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N-(4-(tert-Butyl)phenyl)-2-chloroacetamide
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure, featuring the tert-butyl and chloroacetamide groups, supports the creation of compounds with biological activity in crop protection, enhancing stability and target specificity. Also employed in research settings for the preparation of specialty organic molecules requiring selective reactivity. The chloroacetamide group enables alkylation rea
Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and plant growth regulators. Its structure, featuring the tert-butyl and chloroacetamide groups, supports the creation of compounds with biological activity in crop protection, enhancing stability and target specificity. Also employed in research settings for the preparation of specialty organic molecules requiring selective reactivity. The chloroacetamide group enables alkylation reactions, making it valuable in building complex molecules.
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