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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-Acetyl-3,5-dimethylpyrazine

Cc1cnc(c(n1)C)C(=O)C Request for Quotation
Chemical Name: 2-Acetyl-3,5-dimethylpyrazine
CAS Number: 54300-08-2
Product Number: AG00I9P9(AGN-PC-0WA5Z5)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O
Molecular Weight: 150.1778

Identification/Properties

Properties
BP:
238°C at 760 mmHg
Storage:
Room Temperature;
Refractive Index:
n20/D 1.517(lit.)
Computed Properties
Molecular Weight:
150.181g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
150.079g/mol
Monoisotopic Mass:
150.079g/mol
Topological Polar Surface Area:
42.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
158
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


The 1-(3,5-Dimethylpyrazin-2-yl)ethanone mixture of isomers is a versatile compound widely used in chemical synthesis. This compound serves as a key building block for the production of various pharmaceuticals, fragrances, and agrochemicals. Its unique structure enables it to participate in a range of chemical reactions, leading to the creation of diverse intermediates and final products. In organic synthesis, this mixture of isomers is valued for its ability to introduce specific functional groups and structural motifs into target molecules, allowing chemists to create intricate and specialized compounds for a variety of applications. With its broad utility and reactivity, the 1-(3,5-Dimethylpyrazin-2-yl)ethanone mixture of isomers plays a crucial role in advancing the field of chemical synthesis.