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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)-

2,6-Dimethoxypyrazine

COc1cncc(n1)OC Request for Quotation
Chemical Name: 2,6-Dimethoxypyrazine
CAS Number: 4774-15-6
Product Number: AG006ZQ4(AGN-PC-0KRF31)
Synonyms:
MDL No:
Molecular Formula: C6H8N2O2
Molecular Weight: 140.1399

Identification/Properties

Computed Properties
Molecular Weight:
140.142g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
140.059g/mol
Monoisotopic Mass:
140.059g/mol
Topological Polar Surface Area:
44.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
89.7
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:
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


2,6-Dimethoxypyrazine is a versatile compound widely used in chemical synthesis. As a key building block in organic chemistry, this molecule plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and fragrance ingredients. Its unique structure and reactivity make it an essential component in the synthesis of complex organic compounds. By employing 2,6-Dimethoxypyrazine in reactions, chemists can introduce specific functional groups or enhance the desired properties of the final product. Furthermore, this compound's compatibility with a range of chemical reactions makes it a valuable tool for creating diverse chemical structures with precision and efficiency.