4-carboethoxy-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone

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Reagent Code: #75607
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CAS Number 898757-70-5

science Other reagents with same CAS 898757-70-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.49 g/mol
Formula C₂₄H₂₇NO₅
badge Registry Numbers
MDL Number MFCD03841678
thermostat Physical Properties
Boiling Point 558℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.25g/ml
Storage Room temperature, sealed, ventilated

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of specialized polymers and advanced materials. Its unique structure, featuring a benzophenone moiety and a dioxa-azaspiro component, makes it valuable for creating photoactive compounds. These compounds are often employed in UV-curable coatings, adhesives, and inks, where the benzophenone group acts as a photoinitiator, enabling rapid curing under UV light. Additionally, its spirocyclic structure contributes to the stability and performance of the final product, making it suitable for high-performance applications in the electronics and automotive industries. The compound is also explored in pharmaceutical research for designing drug delivery systems due to its potential to form stable, controlled-release formulations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿58,110.00
inventory 2g
10-20 days ฿96,540.00

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4-carboethoxy-4'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of specialized polymers and advanced materials. Its unique structure, featuring a benzophenone moiety and a dioxa-azaspiro component, makes it valuable for creating photoactive compounds. These compounds are often employed in UV-curable coatings, adhesives, and inks, where the benzophenone group acts as a photoinitiator, enabling rapid curing under UV light. Additionally, its spirocyclic structure contr

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of specialized polymers and advanced materials. Its unique structure, featuring a benzophenone moiety and a dioxa-azaspiro component, makes it valuable for creating photoactive compounds. These compounds are often employed in UV-curable coatings, adhesives, and inks, where the benzophenone group acts as a photoinitiator, enabling rapid curing under UV light. Additionally, its spirocyclic structure contributes to the stability and performance of the final product, making it suitable for high-performance applications in the electronics and automotive industries. The compound is also explored in pharmaceutical research for designing drug delivery systems due to its potential to form stable, controlled-release formulations.

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