4-Bromobenzoyl fluoride

97%

Reagent Code: #151692
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CAS Number 72398-40-4

science Other reagents with same CAS 72398-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.011 g/mol
Formula C₇H₄BrFO
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines and alcohols to form amides and esters, making it valuable in constructing complex molecules. Commonly employed in the preparation of benzoxazepines and other heterocyclic compounds with biological activity. Also utilized in peptide coupling and in the development of functionalized polymers. Its bromine substituent allows for further modification via cross-coupling reactions such as Suzuki or Heck reactions, expanding its utility in medicinal chemistry and materials science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,190.00
inventory 1g
10-20 days ฿5,800.00
inventory 5g
10-20 days ฿20,590.00

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4-Bromobenzoyl fluoride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines and alcohols to form amides and esters, making it valuable in constructing complex molecules. Commonly employed in the preparation of benzoxazepines and other heterocyclic compounds with biological activity. Also utilized in peptide coupling and in the development of functionalized polymers. Its bromine substituent allows for further modification via cross-co

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical and agrochemical industries. It reacts readily with amines and alcohols to form amides and esters, making it valuable in constructing complex molecules. Commonly employed in the preparation of benzoxazepines and other heterocyclic compounds with biological activity. Also utilized in peptide coupling and in the development of functionalized polymers. Its bromine substituent allows for further modification via cross-coupling reactions such as Suzuki or Heck reactions, expanding its utility in medicinal chemistry and materials science.

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