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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)-

1-(5-methoxypyrazin-2-yl)ethanone

COc1ncc(nc1)C(=O)C Request for Quotation
Chemical Name: 1-(5-methoxypyrazin-2-yl)ethanone
CAS Number: 320592-61-8
Product Number: AG00CM4A(AGN-PC-07ACXP)
Synonyms:
MDL No:
Molecular Formula: C7H8N2O2
Molecular Weight: 152.1506

Identification/Properties

Computed Properties
Molecular Weight:
152.153g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
152.059g/mol
Monoisotopic Mass:
152.059g/mol
Topological Polar Surface Area:
52.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
149
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 1-(5-Methoxypyrazin-2-yl)ethanone plays a crucial role in chemical synthesis as it serves as a versatile building block for the creation of various organic compounds. Its unique structure with the pyrazine ring and methoxy group offers opportunities for chemical reactions to occur, facilitating the development of new molecules with diverse properties.In organic synthesis, 1-(5-Methoxypyrazin-2-yl)ethanone can be employed as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials with specific functions. Its reactivity enables the introduction of different functional groups, allowing chemists to modify its structure and generate a range of derivatives tailored for specific applications.Furthermore, this compound can participate in various transformations such as acylation, alkylation, and cross-coupling reactions, making it a valuable component in the construction of complex molecular frameworks. By incorporating 1-(5-Methoxypyrazin-2-yl)ethanone into synthetic routes, chemists can access novel compounds with desired properties for a variety of industrial and academic purposes.