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*For research and further manufacturing use only, not for direct human use.
Structure of 874-87-3
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This sulfane integrates a chloromethyl group and methyl substituent on a phenyl ring, enabling selective functionalization in synthetic workflows. The reactive chloride facilitates nucleophilic substitution under mild conditions, while the sulfur linkage provides stability and compatibility with diverse reaction environments.
(4-(Chloromethyl)phenyl)(methyl)sulfane serves as a versatile bifunctional building block, enabling efficient installation of both aryl and alkyl thioether motifs in synthetic sequences. The chloromethyl group facilitates nucleophilic substitution reactions under mild conditions, while the sulfane functionality offers compatibility with various coupling protocols. Its bench-stable nature and tolerance to common functional groups support reliable use in medicinal chemistry and process development workflows.
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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#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: