1204-75-7 | 3,4-Dihydro-3-oxo-2-quinoxalinecarboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$30.00	$21.00
1g	95%	in stock	$50.00	$35.00
5g	95%	in stock	$185.00	$130.00
25g	95%	in stock	$572.00	$400.00
100g	95%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AB65497
• Chemical Name: 3,4-Dihydro-3-oxo-2-quinoxalinecarboxylic acid
• CAS Number: 1204-75-7
• Molecular Formula: C9H6N2O3
• Molecular Weight: 190.1555
• MDL Number: MFCD00006726
• SMILES: OC(=O)c1nc2ccccc2[nH]c1=O
• NSC Number: 34263

Computed Properties

• Complexity: 311
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 1.2

Upstream Synthesis Route

The compound 3-Oxo-3,4-dihydroquinoxaline-2-carboxylic acid is a versatile building block in chemical synthesis, particularly in the field of medicinal chemistry. Its unique structure makes it a valuable intermediate for the synthesis of various pharmaceutical compounds.One of the key applications of 3-Oxo-3,4-dihydroquinoxaline-2-carboxylic acid is its use in the synthesis of heterocyclic compounds with potential biological activity. By incorporating this compound into a reaction scheme, chemists can access a diverse array of novel molecules with the potential for therapeutic applications. Additionally, the presence of both a ketone and a carboxylic acid moiety in this compound allows for further functionalization, enabling the introduction of different groups to modulate the properties of the final products.Furthermore, 3-Oxo-3,4-dihydroquinoxaline-2-carboxylic acid can serve as a precursor for the synthesis of complex molecules with pharmacological relevance. Through strategic manipulation of its chemical structure, chemists can introduce specific functional groups or stereochemical elements required for the desired biological activity. This compound's versatility and synthetic accessibility make it a valuable tool for the development of new drug candidates and biologically active molecules.

Literature

• Excited state intramolecular proton transfer (ESIPT) in six-coordinated zinc(ii)-quinoxaline complexes with ligand hydrogen bonds: their fluorescent properties sensitive to axial positions.

  Dalton transactions (Cambridge, England : 2003) 20100227

• trans-Bis(dimethyl sulfoxide-kappaO)bis(3-oxo-3,4-dihydroquinoxaline-2-carboxylato-kappa2N1,O2)copper(II).

  Acta crystallographica. Section C, Crystal structure communications 20070501

• Absence of side-effects in the anticonvulsant action of cortically applied antagonists of N-methyl-D-aspartate.

  Brain research 19860514