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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)-

2,6-Difluoro-3-hydroxy-benzonitrile

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Chemical Name: 2,6-Difluoro-3-hydroxy-benzonitrile
CAS Number: 946796-26-5
Product Number: AG01EEFC(AGN-PC-0WAJ3E)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


2,6-Difluoro-3-hydroxybenzonitrile is a versatile compound that finds wide application in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals and agrochemicals due to its unique chemical properties. By incorporating 2,6-Difluoro-3-hydroxybenzonitrile into the synthesis of organic molecules, chemists can introduce specific functionalities and enhance the biological activity of the final products. Additionally, this compound is valued for its ability to participate in various carbon-carbon and carbon-heteroatom bond-forming reactions, making it a valuable tool in the development of complex molecular structures. In the field of medicinal chemistry, 2,6-Difluoro-3-hydroxybenzonitrile plays a crucial role in the design and production of novel drug candidates with improved efficacy and selectivity. This compound's utility extends to the synthesis of advanced materials, dyes, and specialty chemicals, highlighting its significance in modern chemical research and development.