116026-99-4 | (2-Formyl-pyridin-3-yl)-carbamic acid tert-butyl ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$46.00	$33.00
250mg	97%	in stock	$63.00	$45.00
1g	97%	in stock	$138.00	$97.00

Description

• Catalog Number: AA14611
• Chemical Name: (2-Formyl-pyridin-3-yl)-carbamic acid tert-butyl ester
• CAS Number: 116026-99-4
• Molecular Formula: C11H14N2O3
• Molecular Weight: 222.2405
• MDL Number: MFCD04035594
• SMILES: O=Cc1ncccc1NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 260
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 1.8

Upstream Synthesis Route

The tert-Butyl (2-formylpyridin-3-yl)carbamate is a versatile compound widely used in chemical synthesis for its unique properties and applications. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals due to its reactivity and structural attributes. In chemical synthesis, tert-Butyl (2-formylpyridin-3-yl)carbamate exhibits the ability to participate in key reactions such as nucleophilic addition and condensation, enabling the formation of complex structures with high precision and efficiency. Its functional groups play a crucial role in facilitating the assembly of intricate molecular frameworks, making it a valuable tool for organic chemists working on the synthesis of bioactive compounds and functional materials.Furthermore, the introduction of tert-Butyl (2-formylpyridin-3-yl)carbamate into a synthetic pathway can lead to the selective modification of specific sites within a molecule, allowing for tailored chemical transformations and the generation of diverse chemical libraries. Its compatibility with a variety of reaction conditions and functional group manipulations further enhances its utility in synthetic chemistry, making it an indispensable reagent for the preparation of advanced intermediates and final products with desired properties.