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Structure of 6134-55-0
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5-Bromo-1,2,3,4-tetrahydronaphthalene features a bromine substituent at the 5-position of a saturated naphthalene core, providing a reactive handle for cross-coupling and functionalization. This bench-stable, moisture-tolerant intermediate integrates readily into synthetic sequences requiring electron-deficient aromatic systems or steric control in complex molecule assembly.
5-Bromo-1,2,3,4-tetrahydronaphthalene serves as a versatile building block in medicinal chemistry and materials synthesis, enabling efficient functionalization via palladium-catalyzed cross-coupling reactions. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the tetrahydronaphthalene core offers structural rigidity and lipophilicity beneficial for drug-like molecule design. Bench-stable and readily purified by distillation or chromatography, it functions reliably in multi-step syntheses requiring orthogonal reactivity and predictable transformation pathways.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3082
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H319-H410
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Precautionary Statements : P264-P270-P273-P280-P330-P391-P501
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Lot numbers can be found on the outside label of a product: