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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-IODO-5-METHYLPYRAZINE

Cc1ncc(nc1)I Request for Quotation
Chemical Name: 2-IODO-5-METHYLPYRAZINE
CAS Number: 914452-70-3
Product Number: AG00GYOL(AGN-00GYJ1)
Synonyms:
MDL No:
Molecular Formula: C5H5IN2
Molecular Weight: 220.0111

Identification/Properties

Computed Properties
Molecular Weight:
220.013g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
219.95g/mol
Monoisotopic Mass:
219.95g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
76.8
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Iodo-5-methylpyrazine is a valuable chemical compound utilized in organic synthesis for its versatile applications. This compound plays a crucial role in the pharmaceutical industry, where it is commonly used as a building block in the synthesis of various biologically active molecules. Its unique structural properties make it a valuable intermediate in the production of pharmaceutical drugs, agrochemicals, and functional materials. Additionally, 2-Iodo-5-methylpyrazine is frequently employed in the development of flavors and fragrances due to its aromatic characteristics. Its ability to undergo different chemical reactions, such as cross-coupling reactions and nucleophilic substitutions, makes it a suitable candidate for creating complex molecular structures. Whether it is in the lab or industrial scale, 2-Iodo-5-methylpyrazine proves to be an essential component in the realm of chemical synthesis.