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CS-W001157 4
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2-Chloro-5-methoxybenzaldehyde

  • CAS No. 13719-61-4

  • Cat. No. CS-0038044
  • Purity≥97%
  • MDL No.MFCD11845925

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

2-Chloro-5-methoxybenzaldehyde|CS-0038044

Structure of 13719-61-4

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General Information

  • CAS No. 13719-61-4
  • Cat. No. CS-0038044
  • Purity ≥97%
  • MDL No. MFCD11845925
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇ClO₂
  • Molecular Weight 170.59
  • Synonym(s) 2-Chloro-5-Methoxybenzaldehyde(WX622079)
  • SMILES COC1=CC=C(C(=C1)C=O)Cl

Description

2-Chloro-5-methoxybenzaldehyde features a chlorine atom at the ortho position and a methoxy group at the para position relative to the aldehyde, creating a uniquely electron-deficient aromatic scaffold. This configuration enhances reactivity in electrophilic substitution and facilitates coupling reactions under mild conditions. The aldehyde functionality enables direct incorporation into complex molecular architectures via imine formation or reductive amination. Its bench-stable nature supports reliable handling in synthetic workflows.

Application

2-Chloro-5-methoxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles and biologically active scaffolds. Its electron-withdrawing chlorine and methoxy groups provide orthogonal reactivity for selective functionalization, while the aldehyde functionality facilitates imine formation, reductive amination, and coupling reactions. Bench-stable and amenable to standard purification techniques, it functions reliably in multistep synthetic sequences.

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 : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   26.3
  • LogP   2.1611
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   2

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