logo
Home  > Isopropyltriphenylphosphonium iodide

AB24561

24470-78-8 | Isopropyltriphenylphosphonium iodide

Packsize Purity Availability Price Discounted Price    Quantity
5g 95% in stock $9.00 $6.00 -   +
10g 95% in stock $13.00 $9.00 -   +
25g 95% in stock $15.00 $10.00 -   +
100g 95% in stock $42.00 $29.00 -   +
500g 95% in stock $173.00 $122.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB24561
Chemical Name: Isopropyltriphenylphosphonium iodide
CAS Number: 24470-78-8
Molecular Formula: C21H22IP
Molecular Weight: 432.2776
MDL Number: MFCD00031595
SMILES: CC([P+](c1ccccc1)(c1ccccc1)c1ccccc1)C.[I-]
NSC Number: 140615

 

Computed Properties
Complexity: 271  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 23  
Hydrogen Bond Acceptor Count: 1  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • Isopropyltriphenylphosphonium iodide is a versatile reagent commonly used in chemical synthesis for its ability to act as a powerful and selective alkylating agent. Its unique structure and properties make it particularly well-suited for a variety of applications in organic chemistry.In chemical synthesis, Isopropyltriphenylphosphonium iodide is often utilized as a source of isopropyl cations, which can be transferred to nucleophilic substrates to facilitate the formation of new carbon-carbon bonds. This alkylation reaction is highly valuable for the construction of complex organic molecules, allowing chemists to introduce isopropyl groups selectively and efficiently.Additionally, Isopropyltriphenylphosphonium iodide can participate in various transformations such as the Wittig reaction, where it serves as a precursor for the generation of ylides that undergo olefination reactions with aldehydes and ketones. This reactivity expands the synthetic toolbox available to chemists, enabling the preparation of a wide range of functionalized organic compounds.Overall, Isopropyltriphenylphosphonium iodide plays a crucial role in modern organic synthesis by enabling precise control over alkyl group transfer reactions and facilitating the creation of intricate molecular architectures. Its utility in diverse synthetic methodologies underscores its significance as a valuable reagent for the construction of complex organic molecules.
FEATURED PRODUCTS