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Structure of 1914-02-9
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This bench-stable indole derivative features a sterically hindered 3,3-dimethyl substitution that enhances stability and modulates reactivity. The dihydroindole core provides a rigid, electron-rich scaffold ideal for constructing complex heterocycles in synthetic organic chemistry and medicinal chemistry applications.
3,3-Dimethyl-2,3-dihydro-1H-indole serves as a stable, bench-accessible indoline scaffold with enhanced steric protection at the 3-position. Its electron-rich aromatic system facilitates direct functionalization and participates reliably in Pd-catalyzed coupling reactions. The dimethyl substitution improves solubility and reduces unwanted side reactivity, making it well-suited for building complex heterocyclic architectures in medicinal chemistry and process R&D workflows.
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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 : H302-H315-H319-H335
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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: