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CS-W001157 4
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4-Chloro-3-methoxy-5-nitrobenzamide

  • CAS No. 2137975-62-1

  • Cat. No. CS-0148856
  • Molecule weight230.61
  • Purity≥95%
  • MDL No.None

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

4-Chloro-3-methoxy-5-nitrobenzamide|CS-0148856

Structure of 2137975-62-1

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General Information

  • CAS No. 2137975-62-1
  • Cat. No. CS-0148856
  • Purity ≥95%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇ClN₂O₄
  • Molecular Weight 230.61
  • Synonym(s) None
  • SMILES O=C(N)C1=CC([N+]([O-])=O)=C(Cl)C(OC)=C1

Description

4-Chloro-3-methoxy-5-nitrobenzamide features a trifunctional aromatic core with orthogonal reactivity: a chloro group enables palladium-catalyzed coupling, the methoxy moiety offers steric and electronic modulation, and the nitro group provides strong electron-withdrawal. This combination facilitates integration into complex molecular architectures under standard conditions.

Application

4-Chloro-3-methoxy-5-nitrobenzamide serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the aromatic ring due to its complementary electron-withdrawing nitro and chloro groups. The methoxy group provides orthogonal handle for selective derivatization, while the amide functionality offers stability and compatibility with standard coupling reactions. Its bench-stable nature and predictable reactivity facilitate efficient synthesis of heterocyclic scaffolds and API intermediates in multi-step routes.

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

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Computational Chemistry Data

  • TPSA   95.46
  • LogP   1.3557
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   3

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