4,4'-(Piperazine-1,4-diyl)dibenzaldehyde

95%

Reagent Code: #227509
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CAS Number 10159-39-4

science Other reagents with same CAS 10159-39-4

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of conjugated polymers and metal-organic frameworks (MOFs). Its dual aldehyde functionality allows for Schiff base reactions, making it valuable in constructing covalent organic frameworks (COFs) for gas storage or catalysis. Also employed in the preparation of fluorescent sensors due to its ability to form rigid, conjugated structures that exhibit measurable changes in photophysical properties upon binding to specific ions or molecules. Additionally, it serves as a building block in pharmaceutical research for designing bioactive compounds, especially in the development of receptor ligands and enzyme inhibitors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,980.00
250mg
10-20 days ฿5,020.00
1g
10-20 days ฿14,610.00
4,4'-(Piperazine-1,4-diyl)dibenzaldehyde
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Used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of conjugated polymers and metal-organic frameworks (MOFs). Its dual aldehyde functionality allows for Schiff base reactions, making it valuable in constructing covalent organic frameworks (COFs) for gas storage or catalysis. Also employed in the preparation of fluorescent sensors due to its ability to form rigid, conjugated structures that exhibit measurable changes in photophysical properties upon

Used as a key intermediate in the synthesis of advanced organic materials, particularly in the development of conjugated polymers and metal-organic frameworks (MOFs). Its dual aldehyde functionality allows for Schiff base reactions, making it valuable in constructing covalent organic frameworks (COFs) for gas storage or catalysis. Also employed in the preparation of fluorescent sensors due to its ability to form rigid, conjugated structures that exhibit measurable changes in photophysical properties upon binding to specific ions or molecules. Additionally, it serves as a building block in pharmaceutical research for designing bioactive compounds, especially in the development of receptor ligands and enzyme inhibitors.

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