3,5-dichloro-2'-[8-(1,4-dioxa-8-azaspiro[4.5]decyl)methyl]benzophenone

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Reagent Code: #75399
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CAS Number 898756-60-0

science Other reagents with same CAS 898756-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 406.31 g/mol
Formula C₂₁H₂₁Cl₂NO₃
badge Registry Numbers
MDL Number MFCD03842729
thermostat Physical Properties
Boiling Point 569.1℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.36g/ml
Storage Room temperature, sealed, ventilated

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring both a benzophenone core and a spirocyclic dioxa-aza moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of drugs targeting neurological disorders, as the spirocyclic component can enhance binding affinity to specific receptors in the brain. Additionally, its dichloro-substituted benzophenone group is useful in UV-curable coatings and adhesives, where it acts as a photoinitiator to accelerate polymerization processes under UV light. The compound’s versatility also extends to materials science, where it is explored for creating advanced polymers with tailored properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿56,240.00
inventory 2g
10-20 days ฿93,420.00

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3,5-dichloro-2'-[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, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring both a benzophenone core and a spirocyclic dioxa-aza moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of drugs targeting neurological disorders, as the spirocyclic component can enhance binding affinity to specific receptors in the brain. Additionally, its dichloro

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules. Its structure, featuring both a benzophenone core and a spirocyclic dioxa-aza moiety, makes it valuable for constructing pharmacologically active compounds. It is often employed in the development of drugs targeting neurological disorders, as the spirocyclic component can enhance binding affinity to specific receptors in the brain. Additionally, its dichloro-substituted benzophenone group is useful in UV-curable coatings and adhesives, where it acts as a photoinitiator to accelerate polymerization processes under UV light. The compound’s versatility also extends to materials science, where it is explored for creating advanced polymers with tailored properties.

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