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Structure of 533-68-6
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Ethyl 2-bromobutanoate serves as a key alkylating agent in synthetic organic chemistry, featuring a reactive bromine atom at the α-position to the ester group. This configuration enables efficient carbon–carbon bond formation under mild conditions, facilitating the construction of complex molecular architectures. The compound exhibits excellent stability under standard bench protocols and integrates seamlessly into multi-step synthesis workflows.
Ethyl 2-bromobutanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to β-branched alkylated scaffolds. The α-bromo ester functionality facilitates SN₂ reactions with nucleophiles, including amines and thiols, while maintaining compatibility with common protecting groups. Its bench-stable nature and straightforward purification support reliable use in multi-step syntheses, particularly for constructing substituted heterocycles and functionalized carboxylic acid derivatives.
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GHS Pictogram :
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GHS No : GHS02,GHS05,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H302-H315-H318-H335-H412
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P270-P271-P273-P280-P304+P340-P330-P362-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: