34604-60-9 | 5-Hydroxypyrazine-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$13.00	$9.00
5g	97%	in stock	$18.00	$12.00
10g	97%	in stock	$26.00	$18.00
500g	97%	in stock	$1,011.00	$708.00

Description

• Catalog Number: AF59060
• Chemical Name: 5-Hydroxypyrazine-2-carboxylic acid
• CAS Number: 34604-60-9
• Molecular Formula: C5H4N2O3
• Molecular Weight: 140.0969
• MDL Number: MFCD00190599
• SMILES: Oc1cnc(cn1)C(=O)O

Computed Properties

• Complexity: 241
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: -1

Upstream Synthesis Route

5-Oxo-4,5-dihydropyrazine-2-carboxylic acid, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. In organic chemistry, it serves as a key building block in the synthesis of various heterocyclic compounds. Due to its unique structure, $name$ can participate in a variety of reactions to form complex molecules with diverse functionalities.One of the key applications of 5-Oxo-4,5-dihydropyrazine-2-carboxylic acid is in the formation of fused heterocyclic systems through cyclization reactions. By utilizing its reactive carbonyl group and nitrogen atom, this compound can undergo condensation reactions with different nucleophiles or electrophiles, leading to the formation of novel heterocycles. These heterocyclic compounds are crucial in pharmaceutical research and drug discovery as they often exhibit potent biological activities.Moreover, 5-Oxo-4,5-dihydropyrazine-2-carboxylic acid can also be employed as a starting material for the synthesis of peptidomimetics and bioconjugates. Its carboxylic acid group allows for the introduction of various functional groups via traditional peptide coupling reactions, enabling the modification of biomolecules for specific purposes such as drug delivery or protein engineering.Overall, 5-Oxo-4,5-dihydropyrazine-2-carboxylic acid plays a significant role in chemical synthesis by enabling the construction of diverse molecular scaffolds and functionalized compounds with potential applications in medicinal chemistry, material science, and beyond.

Literature

• Acid-base characterization of 5-hydroxypyrazine-2-carboxylic acid and the role of ionic equilibria in the optimization of some process conditions for its biocatalytic production.

  Analytical and bioanalytical chemistry 20051001

• Investigation of the effects of concomitant caffeine administration on the metabolic disposition of pyrazinamide in rats.

  Biopharmaceutics & drug disposition 20020701