1057650-80-2 | tert-Butyl (2-amino-3-pyridinyl)methylcarbamate

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	1 week	$501.00	$351.00
100mg	95%	1 week	$702.00	$492.00
250mg	95%	1 week	$968.00	$678.00
500mg	95%	1 week	$1,480.00	$1,036.00
1g	95%	1 week	$1,877.00	$1,314.00

Description

• Catalog Number: AW41028
• Chemical Name: tert-Butyl (2-amino-3-pyridinyl)methylcarbamate
• CAS Number: 1057650-80-2
• Molecular Formula: C11H17N3O2
• Molecular Weight: 223.2716
• MDL Number: MFCD16293635
• SMILES: O=C(OC(C)(C)C)NCc1cccnc1N

Upstream Synthesis Route

The tert-Butyl N-[(2-Aminopyridin-3-yl)methyl]carbamate is a versatile compound widely utilized in chemical synthesis as a key building block for the preparation of various organic molecules. With its unique structural features, this compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials.In chemical synthesis, tert-Butyl N-[(2-Aminopyridin-3-yl)methyl]carbamate can be employed as a protecting group for amines, enabling selective manipulation of amine functionalities in complex molecular structures. This protection strategy allows chemists to carry out multiple reactions without unwanted interactions with amine groups, facilitating the synthesis of intricate organic compounds with precise control over regioselectivity and stereochemistry.Furthermore, tert-Butyl N-[(2-Aminopyridin-3-yl)methyl]carbamate serves as a valuable source of nucleophilic nitrogen atoms in various synthetic transformations such as nucleophilic substitution, transition metal-catalyzed cross-coupling reactions, and cyclization reactions. Its presence in the molecular scaffold enhances reactivity and enables the construction of diverse chemical architectures with high efficiency.Overall, the application of tert-Butyl N-[(2-Aminopyridin-3-yl)methyl]carbamate in chemical synthesis plays a crucial role in advancing the field of organic chemistry by enabling the efficient and selective synthesis of complex molecules with tailored properties and functions.