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CS-W001157 4
Total: USD 88.00

2-(2-Bromoethyl)thiophene

  • CAS No. 26478-16-0

  • Cat. No. CS-0217535
  • Purity≥98%
  • MDL No.None

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

2-(2-Bromoethyl)thiophene|CS-0217535

Structure of 26478-16-0

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General Information

  • CAS No. 26478-16-0
  • Cat. No. CS-0217535
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₇BrS
  • Molecular Weight 191.09
  • Synonym(s) 2,2-(Bromoethyl)-Thiophene
  • SMILES C1=CSC(=C1)CCBr

Description

2-(2-Bromoethyl)thiophene features a bromoethyl side chain attached to the thiophene ring, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This configuration supports efficient derivatization for synthetic organic chemistry applications. The molecule exhibits high reactivity at the bromine site with minimal steric hindrance, facilitating rapid incorporation into complex molecular architectures under standard conditions.

Application

2-(2-Bromoethyl)thiophene serves as a versatile bifunctional building block for the synthesis of heterocyclic scaffolds and bioactive molecules. The bromoethyl side chain enables facile nucleophilic substitution, while the thiophene core provides a stable, electron-rich platform for cross-coupling reactions. Its bench-stable nature and compatibility with diverse functional groups make it ideal for iterative synthetic sequences in medicinal chemistry and materials science applications.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3265
Class : 8
Packing Group : Ⅱ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   0
  • LogP   2.6855
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   2

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