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Structure of 1490-25-1
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Methyl 4-chloro-4-oxobutanoate features a reactive β-keto ester scaffold flanked by a chloro substituent, enabling direct functionalization at the carbonyl center. This electrophilic motif integrates readily into synthetic sequences requiring selective alkylation or condensation. The molecule exhibits enhanced stability under standard bench conditions and displays favorable solubility in common organic solvents, streamlining handling in process development workflows.
Methyl 4-chloro-4-oxobutanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to γ-chloro-α-keto ester derivatives. Its electrophilic carbonyl and pendant chloride facilitate nucleophilic substitution and enolization reactions, supporting applications in heterocycle synthesis and functional group interconversions. The compound exhibits good bench stability and is amenable to purification via distillation or column chromatography, making it well-suited for use in multi-step synthetic sequences requiring high reproducibility and scalability.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H227-H290-H314
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Precautionary Statements : P210-P234-P260-P264-P280-P301+P330+P331-P304+P340-P363-P370+P378-P390-P403-P405-P406-P501
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Lot numbers can be found on the outside label of a product: