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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)-

Pyrazine, ethylmethyl-

CCc1nccnc1C Request for Quotation
Chemical Name: Pyrazine, ethylmethyl-
CAS Number: 15707-23-0
Product Number: AG001P72(AGN-PC-0JKJG6)
Synonyms:
MDL No: MFCD00006150
Molecular Formula: C7H10N2
Molecular Weight: 122.1677

Identification/Properties

Properties
BP:
173.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.503(lit.)
Solubility:
sparingly soluble
Computed Properties
Molecular Weight:
122.171g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
122.084g/mol
Monoisotopic Mass:
122.084g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
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


2-Ethyl-3-methylpyrazine is a versatile compound that finds important applications in chemical synthesis, particularly in the perfume and flavor industries. This compound is known for its strong, nutty, and roasted aroma, making it a valuable ingredient in creating savory and delicious scents and tastes. In chemical synthesis, 2-Ethyl-3-methylpyrazine serves as a key building block for the preparation of various flavor and fragrance compounds through reactions such as acylation, alkylation, and condensation. Its unique chemical structure allows it to contribute to the development of complex and aromatic products that enhance the sensory experience of food, beverages, and personal care products. Additionally, the use of 2-Ethyl-3-methylpyrazine in chemical synthesis highlights its significance in the creation of specialized and high-quality fragrances and flavors, showcasing its potential for innovation and creativity in the field of scent and taste creation.