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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)-

Pyrazinecarbonitrile, 5-methyl-

Cc1cnc(cn1)C#N Request for Quotation
Chemical Name: Pyrazinecarbonitrile, 5-methyl-
CAS Number: 98006-91-8
Product Number: AG0036VU(AGN-PC-0CW4R3)
Synonyms:
MDL No:
Molecular Formula: C6H5N3
Molecular Weight: 119.1240

Identification/Properties

Properties
BP:
247.1°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
119.127g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
119.048g/mol
Monoisotopic Mass:
119.048g/mol
Topological Polar Surface Area:
49.6A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
135
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


5-Methylpyrazine-2-carbonitrile, also known as 5-MPC, is a versatile compound widely used in chemical synthesis. Its primary application lies in the pharmaceutical and agrochemical industries, where it serves as a valuable building block for the synthesis of various biologically active compounds.In chemical synthesis, 5-Methylpyrazine-2-carbonitrile acts as a key intermediate in the production of diverse organic molecules due to its unique reactivity and functional groups. It is commonly employed in the synthesis of heterocyclic compounds, which are vital components in the development of new drugs, pesticides, and other specialized chemicals.Thanks to its structural properties, 5-Methylpyrazine-2-carbonitrile can undergo a variety of chemical reactions such as nucleophilic substitutions, oxidative transformations, and cycloadditions. This flexibility makes it an indispensable tool for chemists seeking to create complex molecular structures efficiently and with high precision.Overall, 5-Methylpyrazine-2-carbonitrile plays a crucial role in advancing chemical synthesis methods and expanding the possibilities for creating novel compounds with potential applications in various industries.