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CS-W001157 4
Total: USD 88.00

IAV-IN-4

  • CAS No. 93-02-7

  • Cat. No. CS-W007635
  • Purity≥97%
  • MDL No.MFCD00003314

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

IAV-IN-4|CS-W007635

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General Information

  • CAS No. 93-02-7
  • Cat. No. CS-W007635
  • Purity ≥97%
  • MDL No. MFCD00003314
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₀O₃
  • Molecular Weight 166.17
  • Synonym(s) None
  • SMILES O=CC1=CC(OC)=CC=C1OC

Application

2,5-Dimethoxybenzaldehyde serves as a valuable building block in synthetic organic chemistry, enabling efficient access to substituted aromatic scaffolds. Its ortho-dimethoxy substitution pattern enhances electrophilic reactivity while maintaining bench stability and compatibility with standard functional group manipulations. The aldehyde functionality facilitates nucleophilic additions, condensations, and coupling reactions, making it particularly useful in the synthesis of heterocyclic compounds and complex molecular architectures relevant to medicinal chemistry and materials science.

Synthesis

  • Route1
    • 1,4-Dimethoxybenzene, 99%|CS-1269050
      150-78-7
    • null|null
      109-94-4
    • ~31%
    • null|null
      81722-06-7
    • In-stock
      IAV-IN-4|CS-W007635
      93-02-7

    References

    • Tetrahedron, , vol. 68, # 24 p. 4701 - 4709
  • Route2

    References

    • Lakshmi Kantam; Arundhathi; Likhar, Pravin R.; Damodara Advanced Synthesis and Catalysis, 2009 , vol. 351, # 16 p. 2633 - 2637
  • Route3

    References

    • Shanks, Thomas Elbert; Maleski, Robert Joseph Patent: US2003/199714 A1, 2003 ; Location in patent: Page/Page column 4 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07,GHS08
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H334-H335
Precautionary Statements : P261-P264-P271-P280-P284-P302+P352-P304+P340-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   35.53
  • LogP   1.5163
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   3

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