tert-Butyl bis(oxazol-4-ylmethyl)carbamate

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Reagent Code: #146451
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CAS Number 1646152-48-8

science Other reagents with same CAS 1646152-48-8

blur_circular Chemical Specifications

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Weight 279.29 g/mol
Formula C₁₃H₁₇N₃O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral auxiliary and protecting group in organic synthesis, particularly in asymmetric synthesis of complex molecules. Its oxazoline rings coordinate well with metal catalysts, enabling stereoselective transformations such as alkylations, aldol reactions, and Diels-Alder cycloadditions. The tert-butyloxycarbonyl (Boc) group allows for easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis of pharmaceuticals and natural products. Commonly employed in the development of enantiomerically pure intermediates for drug discovery.

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inventory 5g
10-20 days ฿20,900.00

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tert-Butyl bis(oxazol-4-ylmethyl)carbamate
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Used as a chiral auxiliary and protecting group in organic synthesis, particularly in asymmetric synthesis of complex molecules. Its oxazoline rings coordinate well with metal catalysts, enabling stereoselective transformations such as alkylations, aldol reactions, and Diels-Alder cycloadditions. The tert-butyloxycarbonyl (Boc) group allows for easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis of pharmaceuticals and natural products. Commonly employed in the devel

Used as a chiral auxiliary and protecting group in organic synthesis, particularly in asymmetric synthesis of complex molecules. Its oxazoline rings coordinate well with metal catalysts, enabling stereoselective transformations such as alkylations, aldol reactions, and Diels-Alder cycloadditions. The tert-butyloxycarbonyl (Boc) group allows for easy deprotection under mild acidic conditions, making it valuable in multi-step synthesis of pharmaceuticals and natural products. Commonly employed in the development of enantiomerically pure intermediates for drug discovery.

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