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Structure of 1917-64-2
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5-(Methoxymethyl)furan-2-carbaldehyde features a furan ring with a formyl group at C2 and a methoxymethyl substituent at C5, combining electrophilic reactivity with enhanced solubility. This bifunctional scaffold integrates readily into heterocyclic synthesis, enabling efficient access to complex molecular architectures under standard conditions.
5-(Methoxymethyl)furan-2-carbaldehyde serves as a versatile synthon in heterocyclic synthesis, enabling efficient access to functionalized furan derivatives. The aldehyde group facilitates nucleophilic additions and condensation reactions, while the methoxymethyl substituent offers orthogonal protection and mild deprotection conditions. Its stability under standard reaction protocols and compatibility with diverse functional groups make it a practical building block for medicinal chemistry and materials science applications.
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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 : H303-H313-H333
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: