2-(9-Oxoxanthen-2-yl)propionic Acid 1,8-Diazabicyclo[5.4.0]undec-7-ene Salt

≥98%

Reagent Code: #95489
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CAS Number 1346753-05-6

science Other reagents with same CAS 1346753-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 420.51 g/mol
Formula C₂₅H₂₈N₂O₄
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a reagent for facilitating various chemical reactions. Its unique structure makes it effective in promoting esterification and amidation processes, particularly in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals and fine chemicals, where precise control over reaction conditions is crucial. Additionally, it serves as a catalyst in polymerization reactions, aiding in the production of specialized polymers with tailored properties. Its application extends to research laboratories, where it is used to study reaction mechanisms and optimize synthetic pathways.

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Test Parameter Specification
Appearance White - Very pale yellow crystal - powder
Purity 97.5-100
Elemental Analysis Nitrogen 6.1-7.1%
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,960.00
inventory 50mg
10-20 days ฿3,980.00

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2-(9-Oxoxanthen-2-yl)propionic Acid 1,8-Diazabicyclo[5.4.0]undec-7-ene Salt
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This compound is primarily utilized in organic synthesis as a reagent for facilitating various chemical reactions. Its unique structure makes it effective in promoting esterification and amidation processes, particularly in the synthesis of complex organic molecules. It is often employed in the development of pharmaceuticals and fine chemicals, where precise control over reaction conditions is crucial. Additionally, it serves as a catalyst in polymerization reactions, aiding in the production of specialized polymers with tailored properties. Its application extends to research laboratories, where it is used to study reaction mechanisms and optimize synthetic pathways.
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