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CS-W001157 4
Total: USD 88.00

6-Bromobenzo[b]thiophene-2-carboxylic acid 95%

  • CAS No. 19075-58-2

  • Cat. No. CS-1224023
  • Purity≥95%
  • MDL No.None

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

6-Bromobenzo[b]thiophene-2-carboxylic acid 95%|CS-1224023

Structure of 19075-58-2

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General Information

  • CAS No. 19075-58-2
  • Cat. No. CS-1224023
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₅BrO₂S
  • Molecular Weight 257.10
  • Synonym(s) None
  • SMILES O=C(C1=CC2=C(C=C(C=C2)Br)S1)O

Description

6-Bromobenzo[b]thiophene-2-carboxylic acid (95%) features a brominated heterocyclic core fused with a thiophene ring, delivering a robust platform for cross-coupling reactions. The carboxylic acid group enables direct functionalization or derivatization under standard conditions. This bench-stable, moisture-tolerant reagent integrates seamlessly into synthetic sequences requiring halogenated building blocks with enhanced solubility and reactivity.

Application

6-Bromobenzo[b]thiophene-2-carboxylic acid (95%) serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates derivatization via amide formation or esterification. The compound exhibits excellent bench stability, ease of purification, and compatibility with standard synthetic workflows in medicinal chemistry and process development.

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 : H302
Precautionary Statements : P280-P305+P351+P338

Quality Control

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Computational Chemistry Data

  • TPSA   N/A
  • LogP   N/A
  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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