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Structure of 400720-72-1
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tert-Butyl 4-amino-2-chlorobenzylcarbamate features a bench-stable carbamate protecting group that enables selective deprotection under mild acidic conditions. The para-amino and ortho-chloro substituents provide complementary reactivity for late-stage functionalization in medicinal chemistry. This scaffold integrates readily into peptidomimetic architectures and supports efficient derivatization in synthetic routes requiring orthogonal protection strategies.
tert-Butyl 4-amino-2-chlorobenzylcarbamate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted anilines and heterocyclic scaffolds. The ortho-chloro group facilitates palladium-catalyzed cross-coupling reactions, while the protected amine allows for selective functionalization. Its bench-stable tert-butyl carbamate moiety simplifies purification and enables orthogonal deprotection under mild acidic conditions.
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Lot numbers can be found on the outside label of a product: