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5,7-Dichloro-2,3-dihydro-1H-inden-1-one

  • CAS No. 448193-94-0

  • Cat. No. CS-0465560
  • Purity≥98%
  • MDL No.MFCD09908160

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

5,7-Dichloro-2,3-dihydro-1H-inden-1-one|CS-0465560

Structure of 448193-94-0

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General Information

  • CAS No. 448193-94-0
  • Cat. No. CS-0465560
  • Purity ≥98%
  • MDL No. MFCD09908160
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₆Cl₂O
  • Molecular Weight 201.05
  • Synonym(s) 5,7-Dichloro-2,3-dihydroinden-1-one
  • SMILES C1CC(=O)C2=C(C=C(C=C12)Cl)Cl

Description

5,7-Dichloro-2,3-dihydro-1H-inden-1-one is a chlorinated indenone derivative featuring two electron-withdrawing chlorine atoms at the 5 and 7 positions. This configuration enhances electrophilicity at the carbonyl carbon, enabling efficient nucleophilic addition in synthetic transformations. The saturated indene core provides structural rigidity and stability under standard reaction conditions.

Application

5,7-Dichloro-2,3-dihydro-1H-inden-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted indane and indole scaffolds. Its dichlorinated aromatic core provides enhanced electrophilicity for nucleophilic substitution and facilitates transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.

Synthesis

  • Route1

    References

    • Sharma, Anil K.; Subramani, Amutha V.; Gorman, Christopher B. Tetrahedron, 2007 , vol. 63, # 2 p. 389 - 395
  • Route2
    • 3,5-Dichlorobenzaldehyde Ixazomib  Impurity|CS-0228768
      10203-08-4
    • ~%
    • In-stock
      5,7-Dichloro-2,3-dihydro-1H-inden-1-one|CS-0465560
      448193-94-0

    References

    • Musso, David L.; Orr, G. Faye; Cochran, Felicia R.; Kelley, James L.; Selph, Jeffrey L.; Rigdon, Greg C.; Cooper, Barrett R.; Jones, Michael L. Journal of Medicinal Chemistry, 2003 , vol. 46, # 3 p. 409 - 416
  • Route3

    References

    • Musso, David L.; Orr, G. Faye; Cochran, Felicia R.; Kelley, James L.; Selph, Jeffrey L.; Rigdon, Greg C.; Cooper, Barrett R.; Jones, Michael L. Journal of Medicinal Chemistry, 2003 , vol. 46, # 3 p. 409 - 416

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-H319-H412
Precautionary Statements : P264-P270-P273-P280-P330-P501

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Computational Chemistry Data

  • TPSA   17.07
  • LogP   3.1223
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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