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CS-W001157 4
Total: USD 88.00

4-(Dimethylamino)-1,3-benzenedicarboxaldehyde

  • CAS No. 2845-88-7

  • Cat. No. CS-1262364
  • Purity≥98%
  • MDL No.None

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

4-(Dimethylamino)-1,3-benzenedicarboxaldehyde|CS-1262364

Structure of 2845-88-7

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General Information

  • CAS No. 2845-88-7
  • Cat. No. CS-1262364
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₁NO₂
  • Molecular Weight 177.20
  • Synonym(s) None
  • SMILES O=CC1=CC=C(N(C)C)C(C=O)=C1

Description

4-(Dimethylamino)-1,3-benzenedicarboxaldehyde features a conjugated aromatic core bearing two aldehyde groups and a strongly electron-donating dimethylamino substituent. This combination enables efficient coupling in multicomponent reactions and facilitates rapid assembly of complex heterocycles under mild conditions. The molecule exhibits enhanced solubility and stability in organic solvents, making it well-suited for synthetic applications requiring robust, reactive intermediates.

Application

4-(Dimethylamino)-1,3-benzenedicarboxaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized heterocycles and conjugated systems. Its ortho-aldehyde groups exhibit high reactivity in condensation reactions, while the dimethylamino substituent enhances electron density, facilitating nucleophilic additions and transition-metal-catalyzed couplings. The compound demonstrates bench stability and ease of purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science applications.

Safety Information

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Computational Chemistry Data

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  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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