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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)-

5-​FLUORO-​2-​CHLOROPYRAZINE

Fc1ncc(nc1)Cl Request for Quotation
Chemical Name: 5-​FLUORO-​2-​CHLOROPYRAZINE
CAS Number: 959019-05-7
Product Number: AG01JW3H(AGN-PC-0WAKJ3)
Synonyms:
MDL No:
Molecular Formula: C4H2ClFN2
Molecular Weight: 132.5235

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Chemical Structure


2-Chloro-5-fluoropyrazine is a versatile building block in organic synthesis, commonly used in the pharmaceutical and agrochemical industries. This compound serves as a key intermediate in the preparation of various biologically active molecules due to its functional group compatibility and reactivity. In chemical synthesis, 2-Chloro-5-fluoropyrazine can undergo substitution reactions to introduce different groups at the chloro and fluorine positions, allowing for the creation of diverse chemical structures. Additionally, this compound can participate in coupling reactions to form complex organic compounds with multiple functionalities. Its distinct structure and reactivity make it a valuable component in the synthesis of pharmaceuticals, pesticides, and other fine chemicals.