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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)-

3-bromopyrazine-2-carboxylic acid

OC(=O)c1nccnc1Br Request for Quotation
Chemical Name: 3-bromopyrazine-2-carboxylic acid
CAS Number: 937669-80-2
Product Number: AG00H0XX(AGN-PC-03KWS4)
Synonyms:
MDL No:
Molecular Formula: C5H3BrN2O2
Molecular Weight: 202.9935

Identification/Properties

Computed Properties
Molecular Weight:
202.995g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
201.938g/mol
Monoisotopic Mass:
201.938g/mol
Topological Polar Surface Area:
63.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
142
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-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


3-Bromopyrazine-2-carboxylic acid is a versatile building block in chemical synthesis due to its ability to participate in a variety of reactions. This compound is commonly used in organic synthesis as a precursor for the functionalization of pyrazine rings. It can be employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, 3-Bromopyrazine-2-carboxylic acid can serve as a key intermediate in the preparation of complex molecules by allowing for the introduction of specific functional groups through various synthetic transformations such as Suzuki-Miyaura cross-coupling reactions, nucleophilic substitutions, and palladium-catalyzed cross-coupling reactions. The versatility of this compound makes it a valuable tool for the design and production of new chemical entities with potential applications in multiple industries.