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Structure of 7022-45-9
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2-(Methylthio)benzaldehyde features a strategically positioned methylthio group that enhances electron density at the aromatic ring, facilitating efficient electrophilic substitution. The aldehyde functionality enables direct coupling in cross-coupling and condensation reactions, while the sulfur moiety offers orthogonal reactivity for downstream modifications. This compound serves as a key intermediate in synthesizing bioactive heterocycles and functionalized pharmaceuticals.
2-(Methylthio)benzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of heterocyclic scaffolds and bioactive molecules. Its aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the ortho-methylthio group provides moderate electron donation and compatibility with standard protecting group strategies. The compound exhibits good bench stability and is amenable to purification via distillation or column chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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#: 3334
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: