33332-25-1 | Methyl 5-chloropyrazine-2-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$10.00	$7.00
5g	97%	in stock	$12.00	$9.00
10g	97%	in stock	$20.00	$14.00
25g	97%	in stock	$33.00	$23.00
100g	97%	in stock	$130.00	$91.00

Description

• Catalog Number: AB46538
• Chemical Name: Methyl 5-chloropyrazine-2-carboxylate
• CAS Number: 33332-25-1
• Molecular Formula: C6H5ClN2O2
• Molecular Weight: 172.5691
• MDL Number: MFCD27996773
• SMILES: COC(=O)c1cnc(cn1)Cl
• NSC Number: 723999

Computed Properties

• Complexity: 154
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• XLogP3: 0.5

Upstream Synthesis Route

Methyl 5-Chloropyrazine-2-Carboxylate is a versatile compound that finds important applications in chemical synthesis as a key building block in the creation of various complex organic molecules. This compound serves as a valuable intermediate in the pharmaceutical and agrochemical industries, where it is utilized in the synthesis of biologically active compounds.In chemical synthesis, Methyl 5-Chloropyrazine-2-Carboxylate can be employed as a starting material in the production of heterocyclic compounds through various synthetic routes such as nucleophilic substitution, oxidation, and reduction reactions. Its unique structure and reactivity enable the introduction of functional groups at specific positions, allowing for the modification of the molecular properties of the final products.Furthermore, Methyl 5-Chloropyrazine-2-Carboxylate can participate in cross-coupling reactions, cyclization processes, and other advanced synthetic methodologies to access diverse chemical scaffolds with potential applications in drug discovery, materials science, and other fields requiring the preparation of complex organic compounds. Its ability to undergo selective transformations under controlled conditions makes it a valuable tool for chemists seeking to access novel molecular structures for various purposes.

Literature

• Quantitative structure-activity relationships for the in vitro antimycobacterial activity of pyrazinoic acid esters.

  Journal of medicinal chemistry 19960816

• Pyrazinoic acid esters with broad spectrum in vitro antimycobacterial activity.

  Journal of medicinal chemistry 19950929