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Structure of 93989-32-3
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2-Bromo-1-phenylnaphthalene features a bromine atom appended to the naphthalene core, enabling direct incorporation into cross-coupling reactions. The phenyl substituent enhances π-conjugation and electronic modulation, while the molecule exhibits bench-stable handling characteristics under standard conditions. This structure serves as a key intermediate for functionalized polycyclic scaffolds in synthetic organic chemistry.
2-Bromo-1-phenylnaphthalene serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and polyaromatic scaffolds. Its bromine substituent exhibits high reactivity in palladium-catalyzed coupling processes, while the rigid naphthalene core provides structural stability and favorable electronic properties for downstream functionalization. The compound demonstrates excellent bench stability and is readily purified by recrystallization, making it well-suited for reproducible synthetic workflows in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07,GHS08,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H319-H372-H410
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Precautionary Statements : P260-P264-P270-P273-P280-P330-P391-P501
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Lot numbers can be found on the outside label of a product: