6-bromo-3-(6-chloro-2-oxo-2H-chromene-3-carbonyl)-2H-chromen-2-one

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Reagent Code: #196174
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CAS Number 943825-40-9

science Other reagents with same CAS 943825-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.62 g/mol
Formula C₁₉H₈BrClO₅
thermostat Physical Properties
Boiling Point 662.7±55.0 °C
inventory_2 Storage & Handling
Density 1.757±0.06 g/cm3
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorescent dyes and optoelectronic materials due to its extended conjugated system and halogen substitution. The compound serves in Suzuki and Heck coupling reactions to build complex heterocyclic structures for use in organic semiconductors and sensor technologies. Its coumarin backbone with bromo and chloro groups enables selective functionalization for developing bioactive molecules, including potential antimicrobial and anticancer agents. Also employed in photochemical studies for its light-absorbing properties, making it suitable for UV-absorber formulations and fluorescent probes in imaging applications.

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inventory 5mg
10-20 days ฿21,740.00

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6-bromo-3-(6-chloro-2-oxo-2H-chromene-3-carbonyl)-2H-chromen-2-one
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Used as a key intermediate in the synthesis of fluorescent dyes and optoelectronic materials due to its extended conjugated system and halogen substitution. The compound serves in Suzuki and Heck coupling reactions to build complex heterocyclic structures for use in organic semiconductors and sensor technologies. Its coumarin backbone with bromo and chloro groups enables selective functionalization for developing bioactive molecules, including potential antimicrobial and anticancer agents. Also employed

Used as a key intermediate in the synthesis of fluorescent dyes and optoelectronic materials due to its extended conjugated system and halogen substitution. The compound serves in Suzuki and Heck coupling reactions to build complex heterocyclic structures for use in organic semiconductors and sensor technologies. Its coumarin backbone with bromo and chloro groups enables selective functionalization for developing bioactive molecules, including potential antimicrobial and anticancer agents. Also employed in photochemical studies for its light-absorbing properties, making it suitable for UV-absorber formulations and fluorescent probes in imaging applications.

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