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7-Hydroxy-2-oxo-2H-chromene-3-carbaldehyde

  • CAS No. 277313-50-5

  • Cat. No. CS-0065177
  • Purity≥98%
  • MDL No.MFCD24674744

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

7-Hydroxy-2-oxo-2H-chromene-3-carbaldehyde|CS-0065177

Structure of 277313-50-5

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General Information

  • CAS No. 277313-50-5
  • Cat. No. CS-0065177
  • Purity ≥98%
  • MDL No. MFCD24674744
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₆O₄
  • Molecular Weight 190.15
  • Synonym(s) 7-Hydroxy-2-oxo-2H-1-benzopyran-3-carboxaldehyde
  • SMILES O=CC1=CC2=CC=C(O)C=C2OC1=O

Description

7-Hydroxy-2-oxo-2H-chromene-3-carbaldehyde features a fused chromenone core with strategically positioned hydroxyl and aldehyde groups, enabling direct functionalization in synthetic routes. The electron-rich aromatic system supports efficient coupling reactions, while the carbonyl functionalities offer anchoring points for conjugation. This scaffold delivers high reactivity under mild conditions, making it ideal for constructing complex heterocyclic architectures in medicinal chemistry and natural product synthesis.

Application

7-Hydroxy-2-oxo-2H-chromene-3-carbaldehyde serves as a versatile scaffold for the synthesis of coumarin-based bioactive molecules. Its ortho-hydroxyl and aldehyde functionalities enable facile derivatization via condensation, oxidation, or cyclization reactions. The compound exhibits bench stability and compatibility with standard purification methods, facilitating integration into medicinal chemistry workflows targeting anti-inflammatory and antioxidant agents.

Safety Information

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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

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Computational Chemistry Data

  • TPSA   67.51
  • LogP   1.3111
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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