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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyrazinecarboxylic acid, 5-formyl-, methyl ester

COC(=O)c1cnc(cn1)C=O Request for Quotation
Chemical Name: Pyrazinecarboxylic acid, 5-formyl-, methyl ester
CAS Number: 710322-57-9
Product Number: AG003584(AGN-PC-076TPV)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O3
Molecular Weight: 166.1341

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
166.136g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
166.038g/mol
Monoisotopic Mass:
166.038g/mol
Topological Polar Surface Area:
69.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
184
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 5-formylpyrazine-2-carboxylate is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of complex organic molecules, particularly in the pharmaceutical and agrochemical industries.In chemical synthesis, Methyl 5-formylpyrazine-2-carboxylate can be employed as a key intermediate for the preparation of various heterocyclic compounds and functionalized derivatives. Its aldehyde group is a crucial functional moiety that enables further derivatization through various chemical reactions, such as condensation, reduction, and oxidation processes.Furthermore, the pyrazine ring in Methyl 5-formylpyrazine-2-carboxylate imparts aromaticity and stability to the molecule, making it a favored choice for designing bioactive compounds. Its structural features offer opportunities for molecular modifications to enhance desired properties, such as biological activity or solubility.Overall, the application of Methyl 5-formylpyrazine-2-carboxylate in chemical synthesis demonstrates its significance as a valuable precursor for the efficient and strategic construction of diverse organic compounds with potential applications in drug discovery, material science, and other fields of research.