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CS-W001157 4
Total: USD 88.00

4-Bromoindole

  • CAS No. 52488-36-5

  • Cat. No. CS-D1365
  • Purity≥95%
  • MDL No.MFCD00671502

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

4-Bromoindole|CS-D1365

Structure of 52488-36-5

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General Information

  • CAS No. 52488-36-5
  • Cat. No. CS-D1365
  • Purity ≥95%
  • MDL No. MFCD00671502
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₆BrN
  • Molecular Weight 196.04
  • Synonym(s) 4-Bromo-1H-indole; 4-Bromoindole
  • SMILES BrC1=CC=CC2=C1C=CN2

Description

3-Azidopropanoic acid NHS ester is an azidopropanoic acid linker that contains an NHS ester group. The azide group can undergo copper-catalyzed Click Chemistry reactions with alkyne, DBCO and BCN. The NHS ester can react with other primary amines to label proteins and antibodies.

Synthesis

  • Route1
    • null|null
      1180007-97-9
    • ~96%
    • In-stock
      4-Bromoindole|CS-D1365
      52488-36-5

    References

    • Mei, Tian-Sheng; Wang, Xisheng; Yu, Jin-Quan Journal of the American Chemical Society, 2009 , vol. 131, # 31 p. 10806 - 10807
  • Route2
    • 1-(4-Bromo-1H-indol-1-yl)-2,2-dimethylpropan-1-one|CS-0623500
      1196981-04-0
    • ~93%
    • In-stock
      4-Bromoindole|CS-D1365
      52488-36-5

    References

    • Ruiz, Miriam; Sanchez, J. Domingo; Lopez-Alvarado, Pilar; Menendez, J. Carlos Tetrahedron, 2012 , vol. 68, # 2 p. 705 - 710
  • Route3
    • null|null
      105205-47-8
    • ~68%
    • In-stock
      4-Bromoindole|CS-D1365
      52488-36-5

    References

    • Moyer, Mikel P.; Shiurba, John F.; Rapoport, Henry Journal of Organic Chemistry, 1986 , vol. 51, # 26 p. 5106 - 5110

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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