2,4,6-Trimethylbenzene-1,3,5-tricarbaldehyde

95%

Reagent Code: #242225
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CAS Number 119198-88-8

science Other reagents with same CAS 119198-88-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.22 g/mol
Formula C₁₂H₁₂O₃
badge Registry Numbers
MDL Number MFCD00981925
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of advanced organic materials, particularly in the production of specialty resins and ligands for catalysis. Its three aldehyde groups allow for multi-point functionalization, making it valuable in constructing porous organic frameworks and covalent organic polymers (COPs). It is also employed in the development of photoactive compounds and sensors due to its rigid aromatic structure and ability to form Schiff bases. Additionally, it serves as a building block in pharmaceuticals and agrochemicals where trimethyl-substituted benzene scaffolds enhance stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,300.00
inventory 1g
10-20 days ฿13,600.00

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2,4,6-Trimethylbenzene-1,3,5-tricarbaldehyde
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Used as a key intermediate in the synthesis of advanced organic materials, particularly in the production of specialty resins and ligands for catalysis. Its three aldehyde groups allow for multi-point functionalization, making it valuable in constructing porous organic frameworks and covalent organic polymers (COPs). It is also employed in the development of photoactive compounds and sensors due to its rigid aromatic structure and ability to form Schiff bases. Additionally, it serves as a building block

Used as a key intermediate in the synthesis of advanced organic materials, particularly in the production of specialty resins and ligands for catalysis. Its three aldehyde groups allow for multi-point functionalization, making it valuable in constructing porous organic frameworks and covalent organic polymers (COPs). It is also employed in the development of photoactive compounds and sensors due to its rigid aromatic structure and ability to form Schiff bases. Additionally, it serves as a building block in pharmaceuticals and agrochemicals where trimethyl-substituted benzene scaffolds enhance stability and bioavailability.

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