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CS-W001157 4
Total: USD 88.00

1,1,2-Trimethyl-1H-benzo[e]indole

  • CAS No. 41532-84-7

  • Cat. No. CS-W015153
  • Purity≥95%
  • MDL No.MFCD00082627

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

1,1,2-Trimethyl-1H-benzo[e]indole|CS-W015153

Structure of 41532-84-7

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General Information

  • CAS No. 41532-84-7
  • Cat. No. CS-W015153
  • Purity ≥95%
  • MDL No. MFCD00082627
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₁₅N
  • Molecular Weight 209.29
  • Synonym(s) None
  • SMILES CC1=NC2=C(C3=CC=CC=C3C=C2)C1(C)C

Description

Substrate in a four-component synthesis of imidazolidines.

Application

1,1,2-Trimethyl-1H-benz[e]indole serves as a robust polycyclic aromatic scaffold for medicinal chemistry and materials science applications. Its fused indole core exhibits enhanced stability and favorable electronic properties, enabling efficient functionalization at key positions. The trimethyl substitution pattern improves solubility and crystallinity, facilitating purification and handling. This compound functions as a versatile building block in the synthesis of heterocyclic systems and advanced organic semiconductors.

Synthesis

  • Route1
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    • Naphthalen-2-ylhydrazine|CS-0216113
      2243-57-4
    • ~%
    • In-stock
      1,1,2-Trimethyl-1H-benzo[e]indole|CS-W015153
      41532-84-7

    References

    • Societe D'etudes et de Recherches Biologiques Patent: US5750722 A1, 1998 ;
  • Route2
    • null|null
      74-88-4
    • ~%
    • In-stock
      1,1,2-Trimethyl-1H-benzo[e]indole|CS-W015153
      41532-84-7

    References

    • Fischer,E.; Steche Chemische Berichte, 1887 , vol. 20, p. 818,2199 Justus Liebigs Annalen der Chemie, 1887 , vol. 242, p. 353

Safety Information

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

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Computational Chemistry Data

  • TPSA   12.36
  • LogP   4.2234
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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