5-(5-Carboxypyridin-2-yl)isophthalic acid

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Reagent Code: #164463
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CAS Number 1261935-37-8

science Other reagents with same CAS 1261935-37-8

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Weight 287.22 g/mol
Formula C₁₄H₉NO₆
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MDL Number MFCD18318419
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key building block in the synthesis of metal-organic frameworks (MOFs), particularly for applications in gas storage, separation, and catalysis. Its rigid aromatic structure and multiple carboxylic acid groups allow for strong coordination with metal ions, enabling the formation of highly porous and thermally stable networks. Also employed in the development of luminescent sensors due to its ability to chelate lanthanide ions, enhancing photophysical properties for detection of small molecules or environmental pollutants. Additionally, finds use in proton-conductive materials for fuel cell technologies owing to its capacity to form hydrogen-bonded networks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿8,260.00
inventory 1g
10-20 days ฿26,660.00

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5-(5-Carboxypyridin-2-yl)isophthalic acid
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Used as a key building block in the synthesis of metal-organic frameworks (MOFs), particularly for applications in gas storage, separation, and catalysis. Its rigid aromatic structure and multiple carboxylic acid groups allow for strong coordination with metal ions, enabling the formation of highly porous and thermally stable networks. Also employed in the development of luminescent sensors due to its ability to chelate lanthanide ions, enhancing photophysical properties for detection of small molecules

Used as a key building block in the synthesis of metal-organic frameworks (MOFs), particularly for applications in gas storage, separation, and catalysis. Its rigid aromatic structure and multiple carboxylic acid groups allow for strong coordination with metal ions, enabling the formation of highly porous and thermally stable networks. Also employed in the development of luminescent sensors due to its ability to chelate lanthanide ions, enhancing photophysical properties for detection of small molecules or environmental pollutants. Additionally, finds use in proton-conductive materials for fuel cell technologies owing to its capacity to form hydrogen-bonded networks.

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