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CS-W001157 4
Total: USD 88.00

Ethyl 3-bromo-5-chloro-1-(phenylsulfonyl)-1H-indole-2-carboxylate

  • CAS No. 881924-59-0

  • Cat. No. CS-0070688
  • Purity≥97%
  • MDL No.MFCD14584970

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

Ethyl 3-bromo-5-chloro-1-(phenylsulfonyl)-1H-indole-2-carboxylate|CS-0070688

Structure of 881924-59-0

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General Information

  • CAS No. 881924-59-0
  • Cat. No. CS-0070688
  • Purity ≥97%
  • MDL No. MFCD14584970
  • Storage Sealed in dry,2-8℃
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₇H₁₃BrClNO₄S
  • Molecular Weight 442.71
  • Synonym(s) ethyl 1-(benzenesulfonyl)-3-bromo-5-chloroindole-2-carboxylate
  • SMILES O=S(N1C(C(OCC)=O)=C(C2=CC(Cl)=CC=C21)Br)(C3=CC=CC=C3)=O

Synthesis

  • Route1
    • Ethyl 5-Chloro-1-(phenylsulfonyl)-1H-indole-2-carboxylate|CS-0765023
      158561-88-7
    • ~91%
    • Ethyl 3-bromo-5-chloro-1-(phenylsulfonyl)-1H-indole-2-carboxylate|CS-0070688
      881924-59-0

    References

    • Alexandre, Francois-Rene; Amador, Agnes; Bot, Stephanie; Caillet, Catherine; Convard, Thierry; Jakubik, Jocelyn; Musiu, Chiara; Poddesu, Barbara; Vargiu, Luana; Liuzzi, Michel; Roland, Arlene; Seifer, Maria; Standring, David; Storer, Richard; Dousson, Cyril B. Journal of Medicinal Chemistry, 2011 , vol. 54, # 1 p. 392 - 395
  • Route2

    References

    • Alexandre, Francois-Rene; Amador, Agnes; Bot, Stephanie; Caillet, Catherine; Convard, Thierry; Jakubik, Jocelyn; Musiu, Chiara; Poddesu, Barbara; Vargiu, Luana; Liuzzi, Michel; Roland, Arlene; Seifer, Maria; Standring, David; Storer, Richard; Dousson, Cyril B. Journal of Medicinal Chemistry, 2011 , vol. 54, # 1 p. 392 - 395

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   65.37
  • LogP   4.4709
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   4

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