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CS-W001157 4
Total: USD 88.00

2-Bromo-6-iodophenol

  • CAS No. 2040-86-0

  • Cat. No. CS-0139109
  • Purity≥97%
  • MDL No.MFCD16999870

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

2-Bromo-6-iodophenol|CS-0139109

Structure of 2040-86-0

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General Information

  • CAS No. 2040-86-0
  • Cat. No. CS-0139109
  • Purity ≥97%
  • MDL No. MFCD16999870
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₄BrIO
  • Molecular Weight 298.90
  • Synonym(s) PHENOL,2-BROMO-6-IODO
  • SMILES OC1=C(C=CC=C1Br)I

Description

2-Bromo-6-iodophenol delivers a dual halogenated aromatic scaffold for precision synthesis, combining bromine and iodine substituents at meta positions to enable selective cross-coupling reactions. This bench-stable phenolic building block facilitates efficient access to complex heterocycles and functionalized aryl systems under standard conditions.

Application

2-Bromo-6-iodophenol serves as a versatile diaryl building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl scaffolds. Its orthogonal halogen reactivity—bromine typically undergoing Suzuki or Stille coupling while iodine participates in Buchwald-Hartwig amination—facilitates sequential functionalization. The phenolic hydroxyl group offers additional handle for derivatization or protection, enhancing synthetic flexibility. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of complex aromatic architectures relevant to medicinal chemistry and materials science.

Safety Information

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GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 1759
Class : 8
Packing Group : Ⅲ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   20.23
  • LogP   2.7593
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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