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Structure of 89331-94-2
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This spirocyclic xanthone integrates a dibutylamino group at the 6' position and a phenylamino substituent at the 2' position, enhancing electron donation and enabling tailored photophysical behavior. The methyl group at the 3' position introduces steric control, while the isobenzofuran-xanthone scaffold provides rigidity and extended conjugation. This structure supports applications in fluorescent probe development and organic optoelectronics.
6'-(Dibutylamino)-3'-methyl-2'-(phenylamino)-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one serves as a versatile spirocyclic scaffold for the synthesis of functionalized xanthene-based dyes and bioactive molecules. Its dibutylamino and phenylamino substituents enable strong electron-donating character, facilitating charge-transfer interactions in photophysical applications. The molecule exhibits bench stability and tolerates standard coupling conditions, enabling efficient derivatization for materials science and medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: