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Structure of 219862-14-3
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tert-Butyl (1,2,3,4-tetrahydroquinolin-3-yl)carbamate serves as a stable, bench-ready nitrogen protecting group for the synthesis of tetrahydroquinoline-based pharmaceutical intermediates. The carbamate moiety enables selective deprotection under mild acidic conditions, preserving sensitive functional groups. This derivative combines enhanced solubility with robust stability during storage and handling.
tert-Butyl (1,2,3,4-tetrahydroquinolin-3-yl)carbamate serves as a versatile nitrogen protecting group in synthetic organic chemistry, enabling selective functionalization at the 3-position of the tetrahydroquinoline core. Its stability under a range of reaction conditions facilitates downstream transformations, including palladium-catalyzed couplings and reductive deprotection. The carbamate moiety offers excellent solubility and ease of purification, making it well-suited for medicinal chemistry campaigns and API intermediate 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 : 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: