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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)-

4,6,8-trichloro-1,7-naphthyridine

Clc1nc(Cl)c2c(c1)c(Cl)ccn2 Request for Quotation
Chemical Name: 4,6,8-trichloro-1,7-naphthyridine
CAS Number: 931100-02-6
Product Number: AG00IHHH(AGN-PC-0JF44L)
Synonyms:
MDL No:
Molecular Formula: C8H3Cl3N2
Molecular Weight: 233.4818

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Chemical Structure


4,6,8-Trichloro-1,7-naphthyridine is a versatile chemical compound widely used in various chemical synthesis processes. Its unique structure and properties make it a valuable building block in organic chemistry. This compound is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its trichloro-substituted naphthyridine ring system allows for diverse functionalization, enabling the creation of complex molecules with specific applications. In organic synthesis, 4,6,8-Trichloro-1,7-naphthyridine serves as a valuable tool for introducing specific functionalities, such as halogen groups, into target compounds. Its use can streamline reaction pathways and facilitate the efficient production of desired molecules with precise structural features. Additionally, its compatibility with a range of reaction conditions and its tunable reactivity make it a preferred choice for chemists working in the field of chemical synthesis.