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Structure of 954-81-4
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N-(5-Bromopentyl)phthalimide features a brominated alkyl chain tethered to the nitrogen of phthalimide, enabling efficient conjugation in synthetic workflows. This electrophilic handle facilitates nucleophilic substitution reactions under mild conditions, offering a reliable route to functionalized derivatives for medicinal chemistry and polymer synthesis.
N-(5-Bromopentyl)phthalimide serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient introduction of both phthalimido and alkyl bromide moieties. The bromide group facilitates nucleophilic substitution reactions, while the phthalimide acts as a robust nitrogen protecting group. Its stability under standard reaction conditions and compatibility with diverse functional groups make it particularly useful for synthesizing heterocyclic scaffolds and peptide analogs via straightforward alkylation protocols.
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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#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H317-H319-H335-H410
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Precautionary Statements : P261-P264-P270-P271-P272-P273-P280-P302+P352-P304+P340-P330-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: