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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)-

Stannane, methylenebis[fluorodioctyl-

CCCCCCCC[Sn](C[Sn](CCCCCCCC)(CCCCCCCC)F)(CCCCCCCC)F Request for Quotation
Chemical Name: Stannane, methylenebis[fluorodioctyl-
CAS Number: 767355-17-9
Product Number: AG003QLX(AGN-PC-00UMD4)
Synonyms:
MDL No:
Molecular Formula: C33H70F2Sn2
Molecular Weight: 742.3077064

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Chemical Structure


Fluoride ionophore I is a specialized compound used in chemical synthesis for its unique ability to selectively bind fluoride ions. This high affinity for fluoride ions makes it a valuable tool in the development of sensors, probes, and other analytical applications. In chemical synthesis, Fluoride ionophore I can be employed to facilitate the selective transport of fluoride ions across membranes, enabling the targeted delivery of these ions in complex reaction systems. This enhances the efficiency of various synthetic processes where fluoride ions play a critical role, such as in organofluorine chemistry or in the preparation of pharmaceuticals and agrochemicals. Through its intricate molecular structure and sophisticated ion recognition properties, Fluoride ionophore I offers chemists a precise and effective means to manipulate and control the behavior of fluoride ions, opening up new possibilities for innovation and discovery in the field of chemical synthesis.