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*For research and further manufacturing use only, not for direct human use.
Structure of 6640-27-3
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2-Chloro-4-methylphenol delivers a strategically positioned chloro group and methyl substituent on the aromatic ring, enabling selective functionalization in synthetic pathways. This electron-deficient phenolic scaffold supports efficient coupling reactions and serves as a key intermediate in agrochemical and pharmaceutical synthesis.
2-Chloro-4-methylphenol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted aromatic scaffolds. Its ortho-chloro and para-methyl functionalities offer predictable reactivity in nucleophilic aromatic substitution and coupling processes. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process-scale synthesis.
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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-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: