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CS-W001157 4
Total: USD 88.00

Iodocyclopropane

  • CAS No. 19451-11-7

  • Cat. No. CS-0197833
  • Purity≥97%
  • MDL No.MFCD20621267

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

Iodocyclopropane|CS-0197833

Structure of 19451-11-7

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General Information

  • CAS No. 19451-11-7
  • Cat. No. CS-0197833
  • Purity ≥97%
  • MDL No. MFCD20621267
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃H₅I
  • Molecular Weight 167.98
  • Synonym(s) Cyclopropyl iodide
  • SMILES IC1CC1

Description

Iodocyclopropane features a strained three-membered ring that imparts high reactivity, enabling efficient cycloadditions and functional group transfers. This bench-stable iodine-containing scaffold integrates readily into synthetic sequences, serving as a key building block for carbocyclic and heterocyclic architectures in medicinal chemistry and materials science.

Application

Iodocyclopropane serves as a valuable cyclopropyl transfer reagent in synthetic organic chemistry, enabling the efficient introduction of cyclopropyl groups into diverse molecular frameworks. Its high reactivity and stability under standard bench conditions facilitate direct functionalization of nucleophiles, including enolates and organometallics, with predictable stereochemical outcomes. Widely used in medicinal chemistry and natural product synthesis, it functions as a key building block for constructing strained ring systems and bioactive scaffolds.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS02,GHS07
Signal Word : Danger
UN#: 1993
Class : 3
Packing Group : Ⅲ
Hazard Statements : H225-H315-H319-H335
Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501

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Computational Chemistry Data

  • TPSA   0
  • LogP   1.5838
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   0

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