5'-(4-Formyl-3-hydroxyphenyl)-3,3''-dihydroxy-[1,1':3',1''-terphenyl]-4,4''-dicarbaldehyde

97%

Reagent Code: #129889
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CAS Number 2244985-34-8

science Other reagents with same CAS 2244985-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 438.43 g/mol
Formula C₂₇H₁₈O₆
thermostat Physical Properties
Boiling Point 664.9±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.389±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used in organic synthesis as a multifunctional building block for constructing complex polyphenolic frameworks. Its aldehyde and hydroxyl groups enable participation in condensation, cyclization, and metal-chelation reactions. Commonly employed in the development of conjugated organic materials for optoelectronic applications, such as organic semiconductors and sensors. Also investigated for use in crosslinking polymers to enhance thermal and mechanical stability. Shows potential in medicinal chemistry due to structural similarity to bioactive polyphenols, supporting research in antioxidants and enzyme inhibitors.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Yellow Powder
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,610.00
250mg
10-20 days ฿6,150.00
5g
10-20 days ฿57,960.00
1g
10-20 days ฿16,570.00
5'-(4-Formyl-3-hydroxyphenyl)-3,3''-dihydroxy-[1,1':3',1''-terphenyl]-4,4''-dicarbaldehyde
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Used in organic synthesis as a multifunctional building block for constructing complex polyphenolic frameworks. Its aldehyde and hydroxyl groups enable participation in condensation, cyclization, and metal-chelation reactions. Commonly employed in the development of conjugated organic materials for optoelectronic applications, such as organic semiconductors and sensors. Also investigated for use in crosslinking polymers to enhance thermal and mechanical stability. Shows potential in medicinal chemistry d

Used in organic synthesis as a multifunctional building block for constructing complex polyphenolic frameworks. Its aldehyde and hydroxyl groups enable participation in condensation, cyclization, and metal-chelation reactions. Commonly employed in the development of conjugated organic materials for optoelectronic applications, such as organic semiconductors and sensors. Also investigated for use in crosslinking polymers to enhance thermal and mechanical stability. Shows potential in medicinal chemistry due to structural similarity to bioactive polyphenols, supporting research in antioxidants and enzyme inhibitors.

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