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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-bromo-3,5-dichloropyrazine

Clc1cnc(c(n1)Cl)Br Request for Quotation
Chemical Name: 2-bromo-3,5-dichloropyrazine
CAS Number: 1206249-40-2
Product Number: AG003AB8(AGN-PC-09RR6T)
Synonyms:
MDL No:
Molecular Formula: C4HBrCl2N2
Molecular Weight: 227.8741

Identification/Properties

Computed Properties
Molecular Weight:
227.87g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
225.87g/mol
Monoisotopic Mass:
225.87g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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-Bromo-3,5-dichloropyrazine is a versatile building block widely used in chemical synthesis for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. This compound is prized for its unique chemical structure, which allows for the selective introduction of functional groups during the synthesis of complex organic molecules.In chemical synthesis, 2-Bromo-3,5-dichloropyrazine serves as a key intermediate in the creation of heterocyclic compounds, which are essential in the development of drugs, dyes, and materials with specific properties. Its ability to undergo substitution reactions makes it a valuable starting material for the introduction of various substituents, enabling chemists to tailor the properties of the final product to meet specific requirements.Furthermore, the presence of bromine and chlorine atoms on the pyrazine ring provides significant synthetic versatility, allowing for further derivatization through cross-coupling reactions, nucleophilic substitutions, and other chemical transformations. This versatility makes 2-Bromo-3,5-dichloropyrazine a valuable tool in the hands of synthetic chemists seeking to access a diverse array of functionalized pyrazine derivatives for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.