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CS-W001157 4
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6-chloro-5-iodo-3-Pyridinamine

  • CAS No. 444902-32-3

  • Cat. No. CS-0008750
  • Purity95+%
  • MDL No.MFCD11977415

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

 6-chloro-5-iodo-3-Pyridinamine|CS-0008750

Structure of 444902-32-3

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General Information

  • CAS No. 444902-32-3
  • Cat. No. CS-0008750
  • Purity 95+%
  • MDL No. MFCD11977415
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₄ClIN₂
  • Molecular Weight 254.46
  • Synonym(s) 6-Chloro-5-iodopyridin-3-amine
  • SMILES ClC1=NC=C(N)C=C1I

Synthesis

  • Route1

    References

    • Dolle, Frederic; Langle, Sandrine; Roger, Gaelle; Fulton, Roger R.; Lagnel-De Bruin, Beatrice; Henderson, David J.; Hinnen, Francoise; Paine, Taliesha; Coster, Mark J.; Valette, Heric; Bottlaender, Michel; Kassiou, Michael Australian Journal of Chemistry, 2008 , vol. 61, # 6 p. 438 - 445
  • Route2

    References

    • Brown, LaVerne L.; Kulkarni, Santosh; Pavlova, Olga A.; Koren, Andrei O.; Mukhin, Alexey G.; Newman, Amy H.; Horti, Andrew G. Journal of Medicinal Chemistry, 2002 , vol. 45, # 13 p. 2841 - 2849
  • Route3
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      7439-89-6
    • In-stock
      2-Chloro-3-iodo-5-nitropyridine|CS-0008749
      25391-60-0
    • ~%
    • In-stock
       6-chloro-5-iodo-3-Pyridinamine|CS-0008750
      444902-32-3

    References

    • Salvati, Mark E.; Balog, James Aaron; Pickering, Dacia A.; Giese, Soren; Fura, Aberra; Li, Wenying; Patel, Ramesh N.; Hanson, Ronald L.; Mitt, Toomas; Roberge, Jacques Y.; Corte, James R.; Spergel, Steven H.; Rampulla, Richard A.; Misra, Raj N.; Xiao, Hai-Yun Patent: US2004/77605 A1, 2004 ; US 20040077605 A1

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS07,GHS09
Signal Word : Danger
UN#: 1759
Class : 8
Packing Group : Ⅲ
Hazard Statements : H302-H318-H400
Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501

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Computational Chemistry Data

  • TPSA   38.91
  • LogP   1.9218
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   0

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