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Structure of 6834-42-0
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2-(3-Methoxyphenyl)acetyl chloride features a benzoyl moiety bearing a methoxy-substituted phenyl ring, enabling selective acylation in synthetic pathways. The acetyl chloride functionality provides high reactivity for amide and ester formation under mild conditions. This compound demonstrates excellent stability during storage and compatibility with common organic solvents, facilitating smooth integration into multi-step synthesis workflows.
2-(3-Methoxyphenyl)acetyl chloride serves as a versatile acylating agent for the efficient installation of a 3-methoxybenzoyl moiety. It enables direct Friedel-Crafts acylation and amide formation under mild conditions, with good functional group tolerance and bench stability. Its reactivity facilitates rapid access to bioactive scaffolds in medicinal chemistry and materials science.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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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 : H314-H335
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Precautionary Statements : P260-P261-P264-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: