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Structure of 4513-56-8
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2-Bromoethyl 2-methylprop-2-enoate, stabilized with MEHQ, features a reactive bromoethyl handle paired with an electron-deficient enoate moiety. This combination enables efficient conjugation in synthetic transformations, particularly in nucleophilic substitution and polymer functionalization workflows. The stabilizing MEHQ prevents premature polymerization while maintaining shelf stability under standard laboratory conditions.
2-Bromoethyl 2-methylprop-2-enoate, stabilized with MEHQ, serves as a versatile alkylating agent and key building block in synthetic organic chemistry. Its α,β-unsaturated ester functionality enables efficient Michael additions and conjugate functionalizations, while the bromoethyl group facilitates nucleophilic substitution reactions under mild conditions. The compound exhibits enhanced bench stability due to MEHQ stabilization, simplifying handling and purification in multi-step syntheses.
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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 : H227-H315-H319
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Precautionary Statements : P210-P264-P280-P302+P352-P362+P364-P370+P378-P403-P501
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Lot numbers can be found on the outside label of a product: