tert-Butyl 5'-bromo-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate

95%

Reagent Code: #75918
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CAS Number 1398609-80-7

science Other reagents with same CAS 1398609-80-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 340 g/mol
Formula C₁₅H₁₈BrNO₃
badge Registry Numbers
MDL Number MFCD22689962
inventory_2 Storage & Handling
Storage 2-8°C, sealed and dry

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecular structures. Its spirocyclic framework and functional groups make it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives. It is also employed in medicinal chemistry research for designing and optimizing drug candidates, especially those targeting central nervous system disorders. Additionally, its unique structure contributes to the study of stereochemistry and conformational analysis in organic molecules.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿4,554.00

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tert-Butyl 5'-bromo-3'H-spiro[azetidine-3,1'-isobenzofuran]-1-carboxylate
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This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecular structures. Its spirocyclic framework and functional groups make it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives. It is also employed in medicinal chemistry research for designing and

This chemical is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecular structures. Its spirocyclic framework and functional groups make it valuable in the development of pharmaceuticals, particularly in the synthesis of biologically active compounds. The bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives. It is also employed in medicinal chemistry research for designing and optimizing drug candidates, especially those targeting central nervous system disorders. Additionally, its unique structure contributes to the study of stereochemistry and conformational analysis in organic molecules.

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