2,5-Dibromoterephthalaldehyde

98%

Reagent Code: #173884
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CAS Number 63525-48-4

science Other reagents with same CAS 63525-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.94 g/mol
Formula C₈H₄Br₂O₂
badge Registry Numbers
MDL Number MFCD11521314
thermostat Physical Properties
Boiling Point 357.396°C
inventory_2 Storage & Handling
Density 2.011g/mL
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of functional organic materials, particularly in the development of conjugated polymers and metal-organic frameworks (MOFs). Its dual aldehyde and bromine functionalities allow for selective cross-coupling reactions, making it valuable in constructing complex molecular architectures for optoelectronic devices. Commonly employed in Suzuki and Heck reactions to build extended π-systems used in organic semiconductors and sensors. Also serves as a building block in covalent organic frameworks (COFs), where its rigid aromatic structure enhances framework stability and porosity. The presence of bromine atoms enables post-synthetic modifications, facilitating the fine-tuning of electronic properties in advanced materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿410.00
inventory 1g
10-20 days ฿1,480.00
inventory 5g
10-20 days ฿5,780.00
inventory 25g
10-20 days ฿24,460.00

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2,5-Dibromoterephthalaldehyde
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Used as a key intermediate in the synthesis of functional organic materials, particularly in the development of conjugated polymers and metal-organic frameworks (MOFs). Its dual aldehyde and bromine functionalities allow for selective cross-coupling reactions, making it valuable in constructing complex molecular architectures for optoelectronic devices. Commonly employed in Suzuki and Heck reactions to build extended π-systems used in organic semiconductors and sensors. Also serves as a building block in

Used as a key intermediate in the synthesis of functional organic materials, particularly in the development of conjugated polymers and metal-organic frameworks (MOFs). Its dual aldehyde and bromine functionalities allow for selective cross-coupling reactions, making it valuable in constructing complex molecular architectures for optoelectronic devices. Commonly employed in Suzuki and Heck reactions to build extended π-systems used in organic semiconductors and sensors. Also serves as a building block in covalent organic frameworks (COFs), where its rigid aromatic structure enhances framework stability and porosity. The presence of bromine atoms enables post-synthetic modifications, facilitating the fine-tuning of electronic properties in advanced materials.

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