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CS-W001157 4
Total: USD 88.00

9-Chloroacridine

  • CAS No. 1207-69-8

  • Cat. No. CS-W014955
  • Purity≥97%
  • MDL No.MFCD00022266

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

9-Chloroacridine|CS-W014955

Structure of 1207-69-8

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General Information

  • CAS No. 1207-69-8
  • Cat. No. CS-W014955
  • Purity ≥97%
  • MDL No. MFCD00022266
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₃H₈ClN
  • Molecular Weight 213.66
  • Synonym(s) 9-chloroacridone
  • SMILES ClC1=C2C=CC=CC2=NC2=CC=CC=C12

Description

9-Chloroacridine was employed as chromogenic reagent in the spectrophotometric method for the quantitative determination of dapsone. It was also used in the synthesis of:series of novel chalcones bearing acridine moiety attached to the amino group in their ring Anew acridine derivatives9-phenoxyacridine and 4-phenoxyfuro[2,3-b]quinoline derivatives

Synthesis

  • Route1

    References

    • Taherpour, Avat Arman; Kvaskoff, David; Bernhardt, Paul V.; Wentrup, Curt Journal of Physical Organic Chemistry, 2010 , vol. 23, # 4 p. 382 - 389
  • Route2
    • Acridone Oxcarbazepine Impurity|CS-0228810
      578-95-0
    • ~96%
    • In-stock
      9-Chloroacridine|CS-W014955
      1207-69-8

    References

    • Qarawi; Carrington; Blagbrough; Moss; Pouton Pharmaceutical Sciences, 1997 , vol. 3, # 5-6 p. 235 - 239
  • Route3
    • Thio-acridone|CS-1297598
      6540-78-9
    • ~%
    • In-stock
      9-Chloroacridine|CS-W014955
      1207-69-8

    References

    • DE122607 ; Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 6, p. 491 Journal fuer Praktische Chemie (Leipzig), , vol. <2> 64, p. 471 Chemische Berichte, , vol. 33, p. 3770

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

Quality Control

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Computational Chemistry Data

  • TPSA   12.89
  • LogP   4.0414
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   0

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