23628-31-1 | 6-Aminopicolinic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$13.00	$9.00
25g	95%	in stock	$45.00	$31.00
50g	95%	in stock	$73.00	$51.00

Description

• Catalog Number: AB24124
• Chemical Name: 6-Aminopicolinic acid
• CAS Number: 23628-31-1
• Molecular Formula: C6H6N2O2
• Molecular Weight: 138.124
• MDL Number: MFCD00233711
• SMILES: Nc1cccc(n1)C(=O)O
• NSC Number: 522596

Computed Properties

• Complexity: 138
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 0.4

Upstream Synthesis Route

6-Aminopicolinic acid is a versatile chemical compound that finds wide applications in chemical synthesis. Due to its unique structure and reactivity, 6-Aminopicolinic acid is commonly used as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and materials. Its amino and carboxylic acid functional groups make it a valuable intermediate for the production of complex organic molecules. In particular, 6-Aminopicolinic acid serves as a precursor in the synthesis of heterocyclic compounds, such as pyridine derivatives, which are essential in drug discovery and development. Additionally, its ability to participate in various organic reactions makes it a valuable reagent in the preparation of new compounds with diverse properties and applications. By incorporating 6-Aminopicolinic acid into chemical reactions, chemists can access a wide range of potential products with enhanced functionalities and structural complexity.

Literature

• Anion-binding properties of a cyclic pseudohexapeptide containing 1,5-disubstituted 1,2,3-triazole subunits.

  The Journal of organic chemistry 20110902

• Formation of a cyclic tetrapeptide mimic by thermal azide-alkyne 1,3-dipolar cycloaddition.

  Chemical communications (Cambridge, England) 20100807

• A cyclopeptide-derived molecular cage for sulfate ions that closes with a click.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20100625

• Selective sensing of sulfate in aqueous solution using a fluorescent bis(cyclopeptide).

  Organic letters 20071206

• Optimization of the binding properties of a synthetic anion receptor using rational and combinatorial strategies.

  Biosensors & bioelectronics 20050515

• A molecular oyster: a neutral anion receptor containing two cyclopeptide subunits with a remarkable sulfate affinity in aqueous solution.

  Journal of the American Chemical Society 20021030