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CS-W001157 4
Total: USD 88.00

7-Bromo-1H-indole

  • CAS No. 51417-51-7

  • Cat. No. CS-W002687
  • Purity≥95%
  • MDL No.MFCD00799492

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

7-Bromo-1H-indole|CS-W002687

Structure of 51417-51-7

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General Information

  • CAS No. 51417-51-7
  • Cat. No. CS-W002687
  • Purity ≥95%
  • MDL No. MFCD00799492
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆BrN
  • Molecular Weight 196.04
  • Synonym(s) None
  • SMILES BrC1=CC=CC2=C1NC=C2

Description

7-Bromoindole is a 7-substituted indole derivative. Its synthesis from 7-bromoindole-2-carboxylic acid has been reported. It has been reported to reduce the production of staphyloxanthin in Staphylococcus aureus.7-Bromoindole may be used in the synthesis of the following:indoledyestuffs8-bromocarboline

Synthesis

  • Route1
    • null|null
      577-19-5
    • null|null
      1826-67-1
    • ~73%
    • In-stock
      7-Bromo-1H-indole|CS-W002687
      51417-51-7

    References

    • Smith III, Amos B.; Kuerti, Laszlo; Davulcu, Akin H.; Young, Shin Cho; Ohmoto, Kazuyuki Journal of Organic Chemistry, 2007 , vol. 72, # 13 p. 4611 - 4620
  • Route2

    References

    • Yamada, Yaeko; Arima, Shiho; Okada, Chiharu; Akiba, Ai; Kai, Toshitsugu; Harigaya, Yoshihiro Chemical and Pharmaceutical Bulletin, 2006 , vol. 54, # 6 p. 788 - 794
  • Route3
    • null|null
      74798-64-4
    • ~85%
    • In-stock
      7-Bromo-1H-indole|CS-W002687
      51417-51-7

    References

    • Glennon, R. A.; Schubert, E.; Jacyno, J. M.; Rosecrans, J. A. Journal of Medicinal Chemistry, 1980 , vol. 23, # 11 p. 1222 - 1226

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-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   15.79
  • LogP   2.9304
  • H_Acceptors   0
  • H_Donors   1
  • Rotatable_Bonds   0

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