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Home  > Hydrogen hexachloroiridate(iv) hydrate

AB74714

110802-84-1 | Hydrogen hexachloroiridate(iv) hydrate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $68.00 $47.00 -   +
250mg 98% in stock $90.00 $63.00 -   +
1g 98% in stock $329.00 $230.00 -   +
5g 98% in stock $1,405.00 $984.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB74714
Chemical Name: Hydrogen hexachloroiridate(iv) hydrate
CAS Number: 110802-84-1
Molecular Formula: Cl6IrO
Molecular Weight: 424.9662
MDL Number: MFCD00011328
SMILES: [Cl-].[Cl-].[Cl-].[Cl-].[Ir+4].Cl.Cl.O

 

Upstream Synthesis Route
  • Dihydrogen hexachloroiridate(IV) xhydrate, also known as H2IrCl6∙xH2O, serves as a valuable chemical reagent in organic synthesis due to its ability to participate in various catalytic reactions. This compound is commonly utilized in the synthesis of complex organic molecules through processes such as hydrogenation, isomerization, and oxidation reactions.One of the key applications of Dihydrogen hexachloroiridate(IV) xhydrate in chemical synthesis is its use as a catalyst in the hydrogenation of unsaturated organic compounds. By utilizing H2IrCl6∙xH2O as a catalyst in hydrogenation reactions, chemists can effectively convert alkenes and alkynes into the corresponding saturated hydrocarbons, providing a versatile method for the reduction of functional groups in organic molecules.Furthermore, Dihydrogen hexachloroiridate(IV) xhydrate plays a crucial role in the isomerization of organic compounds, particularly in the rearrangement of double bonds or functional groups within a molecule. Its catalytic properties enable chemists to selectively isomerize specific bonds, leading to the formation of desired isomeric products with high efficiency and selectivity.Additionally, this compound is instrumental in oxidation reactions, where it can facilitate the conversion of primary and secondary alcohols into aldehydes and ketones. The catalytic activity of H2IrCl6∙xH2O allows for precise control over the oxidation process, enabling chemists to selectively oxidize specific functional groups while minimizing undesired byproducts.Overall, Dihydrogen hexachloroiridate(IV) xhydrate serves as a versatile and effective reagent in chemical synthesis, enabling the synthesis of complex organic molecules through a variety of catalytic reactions. Its unique properties make it an invaluable tool for synthetic chemists seeking to develop novel and efficient synthetic routes for the production of pharmaceuticals, agrochemicals, and fine chemicals.
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