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Pharmaceutical Intermediates (3-Bromopropyl) Triphenylphosphonium Bromide CAS 3607-17-8

(3-Bromopropyl)Triphenylosphonium bromide a versatile organic compound with a unique structure containing a phosphonium cation and a bromide anion. It is widely used in various chemical reactions and synthesis due to its reactivity and stability. This compound has gained attention in organic chemistry research and finds applications in several fields.
  • CAS #:

    3607-17-8
  • Certificates:

    ISO | Kosher | Halal |
  • Specifications:

    99%
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    L/C,T/T,D/P,Western Union,Paypal,Money Gram

Products Description

(3-Bromopropyl)Triphenylosphonium bromide a versatile organic compound with a unique structure containing a phosphonium cation and a bromide anion. It is widely used in various chemical reactions and synthesis due to its reactivity and stability. This compound has gained attention in organic chemistry research and finds applications in several fields.

Function

The primary function of (3-Bromopropyl)Triphenylphosphonium bromide is its ability to act as a valuable building block in organic synthesis. It serves as a source of the nucleophilic phosphonium carbanion, which can readily undergo substitution and addition reactions with various electrophilic species. The bromide counterion enhances the reactivity and provides stability to the phosphonium cation, facilitating its participation in different reactions.

Application
  1. As a versatile synthetic reagent: (3-Bromopropyl)Triphenylphosphonium bromide is commonly employed in the preparation of complex molecules through a range of reactions, including nucleophilic substitution, Wittig reaction, and Michael addition. It enables the introduction of the phosphonium group into target molecules, offering synthetic chemists a powerful tool for molecular modification.

  2. Catalyst and ligand precursor: The phosphonium group in this compound can serve as a catalyst or ligand in various chemical transformations. It can participate in catalytic reactions such as cross-coupling reactions, C-H activation, and asymmetric transformations, thereby enabling the selective formation of desired products. Additionally, the bromide anion can be exchanged with other anions to tailor the properties of the catalyst or ligand.

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