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CS-W001157 4
Total: USD 88.00

3-Azatricyclo[4.2.1.02,5]non-7-en-4-one

  • CAS No. 14735-70-7

  • Cat. No. CS-0038706
  • Purity≥97%
  • MDL No.None

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

3-Azatricyclo[4.2.1.02,5]non-7-en-4-one|CS-0038706

Structure of 14735-70-7

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General Information

  • CAS No. 14735-70-7
  • Cat. No. CS-0038706
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₉NO
  • Molecular Weight 135.16
  • Synonym(s) NORBORNENE AZETIDINONE
  • SMILES C1=C[C@@H]2C[C@H]1C3C2NC3=O

Synthesis

  • Route1
    • null|null
      1189-71-5
    • null|null
      121-46-0
    • ~83%
    • In-stock
      3-Azatricyclo[4.2.1.02,5]non-7-en-4-one|CS-0038706
      14735-70-7

    References

    • Anadys Pharmaceuticals, Inc. Patent: US2009/306057 A1, 2009 ; Location in patent: Page/Page column 78-79 ;
  • Route2
    • null|null
      14805-30-2
    • ~%
    • In-stock
      3-Azatricyclo[4.2.1.02,5]non-7-en-4-one|CS-0038706
      14735-70-7

    References

    • Allwein, Shawn P.; Roemmele, Renee C.; Haley, James J.; Mowrey, Dale R.; Petrillo, Daniel E.; Reif, James J.; Gingrich, Diane E.; Bakale, Roger P. Organic Process Research and Development, 2012 , vol. 16, # 1 p. 148 - 155
  • Route3
    • null|null
      121-46-0
    • ~%
    • In-stock
      3-Azatricyclo[4.2.1.02,5]non-7-en-4-one|CS-0038706
      14735-70-7

    References

    • Allwein, Shawn P.; Roemmele, Renee C.; Haley, James J.; Mowrey, Dale R.; Petrillo, Daniel E.; Reif, James J.; Gingrich, Diane E.; Bakale, Roger P. Organic Process Research and Development, 2012 , vol. 16, # 1 p. 148 - 155

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   29.1
  • LogP   0.3069
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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