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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)-

Aluminate(3-), hexafluoro-, tripotassium, (OC-6-11)-

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Chemical Name: Aluminate(3-), hexafluoro-, tripotassium, (OC-6-11)-
CAS Number: 13775-52-5
Product Number: AG01E6N2(AGN-PC-0PLO4R)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

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Chemical Structure


The aluminate(3-), hexafluoro-, potassium (1:3), (OC-6-11)- compound is widely utilized in chemical synthesis as a versatile reagent. It serves as a key component in many reactions due to its unique properties and capabilities. This compound is particularly valuable in organic synthesis for its ability to serve as a strong base, facilitating various complex transformations such as deprotonation and nucleophilic substitution reactions. Its hexafluoroaluminate structure enhances its stability and reactivity, making it highly efficient in promoting a wide range of synthetic processes. Additionally, the presence of potassium ions in the compound further enhances its reactivity and selectivity, allowing for precise control over reactions. Overall, the aluminate(3-), hexafluoro-, potassium (1:3), (OC-6-11)- compound plays a crucial role in advancing chemical synthesis by enabling the efficient and precise manipulation of molecules to create new and valuable compounds.