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CS-W001157 4
Total: USD 88.00

(Iodomethyl)triphenylphosphonium iodide

  • CAS No. 3020-28-8

  • Cat. No. CS-0040930
  • Purity≥97%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

(Iodomethyl)triphenylphosphonium iodide|CS-0040930

Structure of 3020-28-8

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General Information

  • CAS No. 3020-28-8
  • Cat. No. CS-0040930
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₁₇I₂P
  • Molecular Weight 530.12
  • Synonym(s) (Iodomethyl)(triphenyl)phosphonium iodide
  • SMILES IC[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[I-]

Description

(Iodomethyl)triphenylphosphonium iodide delivers a reactive iodomethyl group tethered to a stable phosphonium center, enabling efficient alkylation under mild conditions. This bench-stable reagent integrates readily into synthetic sequences requiring selective C-alkylation, particularly in the construction of phosphonium salts and functionalized organic frameworks.

Application

(Iodomethyl)triphenylphosphonium iodide serves as a reliable source of iodomethyl electrophiles in organic synthesis, enabling efficient alkylation reactions under mild conditions. Its stability and ease of handling make it well-suited for bench-scale applications, particularly in the construction of functionalized alkylphosphonium salts and heterocyclic scaffolds via nucleophilic substitution.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   0
  • LogP   1.377
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   4

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