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CS-W001157 4
Total: USD 88.00

1-Indanone

  • CAS No. 83-33-0

  • Cat. No. CS-W004333
  • Purity≥98%
  • MDL No.MFCD00003785

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

1-Indanone|CS-W004333

Structure of 83-33-0

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General Information

  • CAS No. 83-33-0
  • Cat. No. CS-W004333
  • Purity ≥98%
  • MDL No. MFCD00003785
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₈O
  • Molecular Weight None
  • Synonym(s) α-Hydrindone
  • SMILES O=C1CCC2=C1C=CC=C2

Description

1-Naphthyl phosphate disodium salt hydrate is used as an organic chemical synthesis intermediate.

Application

1-Indanone serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of fused bicyclic scaffolds and heterocycles. Its ketone functionality facilitates nucleophilic additions, enolization, and transition-metal-catalyzed couplings. The molecule exhibits excellent bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.

Synthesis

  • Route1
    • null|null
      54509-73-8
    • Phenyl(trimethylsilyl)methanone|CS-1671695
      5908-41-8
    • ~%
    • null|null
      27397-33-7
    • In-stock
      1-Indanone|CS-W004333
      83-33-0

    References

    • Journal of Organometallic Chemistry, , vol. 464, # 2 p. 171 - 182
  • Route2
    • Phenyl(trimethylsilyl)methanone|CS-1671695
      5908-41-8
    • null|null
      74-86-2
    • ~%
    • null|null
      480-90-0
    • In-stock
      1-Indanone|CS-W004333
      83-33-0

    References

    • Journal of Organometallic Chemistry, , vol. 464, # 2 p. 171 - 182
  • Route3

    References

    • Journal of the Chemical Society. Perkin Transactions 1, , # 3 p. 402 - 415

Safety Information

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GHS Pictogram : N/A
GHS No : N/A
Signal Word : N/A
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

Quality Control

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Computational Chemistry Data

  • TPSA   17.07
  • LogP   1.8155
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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