4-(tert-Butyl)benzoyl fluoride

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Reagent Code: #151691
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CAS Number 174579-99-8

science Other reagents with same CAS 174579-99-8

blur_circular Chemical Specifications

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Weight 180.222 g/mol
Formula C₁₁H₁₃FO
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its acyl fluoride group is highly reactive toward nucleophiles, making it valuable for forming amide and ester bonds under mild conditions. Commonly employed in the synthesis of liquid crystals and functional materials due to the stability imparted by the tert-butylphenyl moiety. Also utilized in Friedel-Crafts acylation reactions where a bulky aromatic acyl group is required. Its volatility and reactivity make it suitable for use in controlled reactions under anhydrous conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,540.00
inventory 1g
10-20 days ฿5,930.00
inventory 5g
10-20 days ฿23,930.00

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4-(tert-Butyl)benzoyl fluoride
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its acyl fluoride group is highly reactive toward nucleophiles, making it valuable for forming amide and ester bonds under mild conditions. Commonly employed in the synthesis of liquid crystals and functional materials due to the stability imparted by the tert-butylphenyl moiety. Also utilized in Friedel-Crafts acylation reactions where a bulky aromatic acyl group is required. Its volatilit

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its acyl fluoride group is highly reactive toward nucleophiles, making it valuable for forming amide and ester bonds under mild conditions. Commonly employed in the synthesis of liquid crystals and functional materials due to the stability imparted by the tert-butylphenyl moiety. Also utilized in Friedel-Crafts acylation reactions where a bulky aromatic acyl group is required. Its volatility and reactivity make it suitable for use in controlled reactions under anhydrous conditions.

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