logo
Home  > Sodium 10b-Ffluoro-​1,​3,​4,​4a,​4b,​5,​6,​10a,​10b,​11,​12,​12a-​dodecahydro-​1,​11-​dihydroxy-​3,​10a,​12a-​trimethyl-​1-​[(phosphonooxy)​methyl]​-2,​8-​chrysenedione

BJ78271

1201919-18-7 | Sodium 10b-Ffluoro-​1,​3,​4,​4a,​4b,​5,​6,​10a,​10b,​11,​12,​12a-​dodecahydro-​1,​11-​dihydroxy-​3,​10a,​12a-​trimethyl-​1-​[(phosphonooxy)​methyl]​-2,​8-​chrysenedione

Availability
Typically In Stock

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: BJ78271
Chemical Name: Sodium 10b-Ffluoro-​1,​3,​4,​4a,​4b,​5,​6,​10a,​10b,​11,​12,​12a-​dodecahydro-​1,​11-​dihydroxy-​3,​10a,​12a-​trimethyl-​1-​[(phosphonooxy)​methyl]​-2,​8-​chrysenedione
CAS Number: 1201919-18-7
Molecular Formula: C22H28FNa2O8P
Molecular Weight: 516.4046
SMILES: [Na]OP(=O)(OC[C@]1(O)C(=O)[C@@H](C)C[C@@H]2[C@]1(C)C[C@H](O)[C@]1([C@H]2CCC2=CC(=O)C=C[C@]12C)F)O[Na]

 

Upstream Synthesis Route
  • Sodium 10b-fluoro-1,3,4,4a,4b,5,6,10a,10b,11,12,12a-dodecahydro-1,11-dihydroxy-3,10a,12a-trimethyl-1-[(phosphonooxy)methyl]-2,8-chrysenedione is a versatile compound widely used in chemical synthesis processes. Its unique structure and properties make it a valuable reagent in the synthesis of complex organic molecules and pharmaceutical intermediates. This compound serves as a key building block for the construction of intricate molecular structures due to its ability to undergo various chemical transformations, such as alkylation, oxidation, and condensation reactions. Through strategic manipulation of its functional groups, this compound enables chemists to access diverse chemical scaffolds and achieve challenging molecular architectures efficiently. In addition, its fluorinated moiety can impart valuable properties to the final products, such as improved metabolic stability and enhanced biological activity in drug discovery applications.
FEATURED PRODUCTS