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Abemaciclib Impurity 1

  • CAS No. 1231930-33-8

  • Cat. No. CS-M2089
  • Purity≥98%
  • MDL No.MFCD16660227

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

Abemaciclib Impurity 1|CS-M2089

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General Information

  • CAS No. 1231930-33-8
  • Cat. No. CS-M2089
  • Purity ≥98%
  • MDL No. MFCD16660227
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₂BrFN₂
  • Molecular Weight 271.13
  • Synonym(s) 6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole
  • SMILES CC1=NC2=C(F)C=C(Br)C=C2N1C(C)C

Description

6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole features a sterically hindered imidazole core with complementary halogen and alkyl substituents, enabling selective coupling in late-stage functionalization. The electron-deficient aryl ring facilitates palladium-catalyzed cross-coupling reactions under standard conditions, while the isopropyl and methyl groups enhance solubility and stability during synthesis.

Application

6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole serves as a versatile building block for the synthesis of bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its bromine and fluorine substituents. Its isopropyl and methyl groups enhance steric and electronic modulation, facilitating selective functionalization in medicinal chemistry applications. The compound exhibits bench stability and compatibility with standard purification protocols, making it well-suited for scalable synthesis workflows.

Synthesis

  • Route1

    References

    • US2010/160340 A1, ; Page/Page column 10 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   17.82
  • LogP   3.82722
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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