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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)-

2(1H)-Pyrazinone, 6-methyl-

Cc1cncc(=O)[nH]1 Request for Quotation
Chemical Name: 2(1H)-Pyrazinone, 6-methyl-
CAS Number: 20721-18-0
Product Number: AG002IWL(AGN-PC-0JP8DF)
Synonyms:
MDL No: MFCD08705761
Molecular Formula: C5H6N2O
Molecular Weight: 110.1139

Identification/Properties

Properties
MP:
152 - 157 °C
BP:
376.2°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
110.116g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
110.048g/mol
Monoisotopic Mass:
110.048g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
169
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methylpyrazin-2-ol, also known as 6-methyl-2-pyrazinol, is a versatile organic compound that finds significant application in chemical synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. 6-Methylpyrazin-2-ol can be utilized as a key intermediate in the synthesis of biologically active compounds due to its unique chemical structure. Its reactivity allows for the formation of various substituted derivatives through functional group transformations such as acylation, alkylation, and nucleophilic substitution reactions. In addition, 6-Methylpyrazin-2-ol can participate in heterocyclic chemistry, enabling the construction of complex molecular frameworks with diverse properties. Its ability to undergo condensation reactions with carbonyl compounds or amino acids opens up pathways for the creation of novel heterocyclic structures with potential biological activities.Overall, the versatile nature of 6-Methylpyrazin-2-ol makes it a valuable tool in the hands of synthetic chemists seeking to develop innovative molecules for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.