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CS-W001157 4
Total: USD 88.00

2-Chloro-1-methyl-1h-indole-3-carbaldehyde

  • CAS No. 24279-74-1

  • Cat. No. CS-0214986
  • Purity≥98%
  • MDL No.None

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

2-Chloro-1-methyl-1h-indole-3-carbaldehyde|CS-0214986

Structure of 24279-74-1

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General Information

  • CAS No. 24279-74-1
  • Cat. No. CS-0214986
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₈ClNO
  • Molecular Weight 193.63
  • Synonym(s) 2-chloro-1-methyl-indole-3-carbaldehyde
  • SMILES CN1C2=CC=CC=C2C(=C1Cl)C=O

Synthesis

  • Route1
    • In-stock
      2-Chloro-1H-indole-3-carbaldehyde|CS-0156034
      5059-30-3
    • null|null
      74-88-4
    • ~99%
    • In-stock
      2-Chloro-1-methyl-1h-indole-3-carbaldehyde|CS-0214986
      24279-74-1

    References

    • Aventis Pharmaceuticals Inc. Patent: US2005/54631 A1, 2005 ; Location in patent: Page/Page column 17 ;
  • Route2
    • In-stock
      1-Methylindolin-2-one|CS-W013308
      61-70-1
    • null|null
      68-12-2
    • ~78%
    • In-stock
      2-Chloro-1-methyl-1h-indole-3-carbaldehyde|CS-0214986
      24279-74-1

    References

    • Zhang, Yiming; Wang, Ren; Shi, Zongjun; Zhang, Wei Synthesis, 2011 , # 11 p. 1711 - 1716
  • Route3
    • null|null
      77-78-1
    • In-stock
      2-Chloro-1H-indole-3-carbaldehyde|CS-0156034
      5059-30-3
    • ~85%
    • In-stock
      2-Chloro-1-methyl-1h-indole-3-carbaldehyde|CS-0214986
      24279-74-1

    References

    • Monge; Palop; Ramirez; Font; Fernandez-Alvarez European Journal of Medicinal Chemistry, 1991 , vol. 26, # 2 p. 179 - 188

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-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   22
  • LogP   2.6442
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   1

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