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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)-

methyl 6-chloro-3-methylpyrazine-2-carboxylate

Cc1ncc(nc1C(=O)OC)Cl Request for Quotation
Chemical Name: methyl 6-chloro-3-methylpyrazine-2-carboxylate
CAS Number: 1166831-45-3
Product Number: AG000CZH(AGN-PC-0C8EEE)
Synonyms:
MDL No:
Molecular Formula: C7H7ClN2O2
Molecular Weight: 186.5957

Identification/Properties

Computed Properties
Molecular Weight:
186.595g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
186.02g/mol
Monoisotopic Mass:
186.02g/mol
Topological Polar Surface Area:
52.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
177
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 6-chloro-3-methylpyrazine-2-carboxylate is a versatile chemical compound that finds wide application in organic synthesis. Its strategic molecular structure allows it to serve as a key building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Specifically, the incorporation of this compound in chemical synthesis processes enables the introduction of essential chloro and methyl functional groups with precision, facilitating the synthesis of complex molecules with desired pharmacological or biological activities. Due to its high reactivity and compatibility with a range of reaction conditions, Methyl 6-chloro-3-methylpyrazine-2-carboxylate has become a valuable tool for medicinal chemists, agrochemists, and researchers in the field of organic synthesis seeking to design and produce novel compounds for various applications.