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CS-W001157 4
Total: USD 88.00

2-Chloro-6-iodoaniline

  • CAS No. 84483-28-3

  • Cat. No. CS-W004944
  • Purity≥98%
  • MDL No.MFCD08443948

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

2-Chloro-6-iodoaniline|CS-W004944

Structure of 84483-28-3

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General Information

  • CAS No. 84483-28-3
  • Cat. No. CS-W004944
  • Purity ≥98%
  • MDL No. MFCD08443948
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅ClIN
  • Molecular Weight 253.47
  • Synonym(s) Benzenamine, 2-chloro-6-iodo-
  • SMILES NC1=C(I)C=CC=C1Cl

Description

2-Chloro-6-iodoaniline features a dual halogenated aromatic core, combining electron-withdrawing chlorine and iodine substituents at ortho positions relative to the amine group. This configuration enables selective cross-coupling reactions in late-stage functionalization, particularly in palladium-catalyzed processes. The molecule exhibits enhanced stability under standard bench conditions and facilitates efficient incorporation into complex heterocyclic scaffolds.

Application

2-Chloro-6-iodoaniline serves as a versatile building block for the synthesis of functionalized aromatic scaffolds, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The chloro and iodo groups facilitate sequential transformations, with the iodo moiety typically reacting first under mild conditions. Its stability under standard bench handling and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and process development workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H301-H319
Precautionary Statements : P264-P270-P280-P330-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   26.02
  • LogP   2.5268
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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