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

  • CAS No. 2137975-63-2

  • Cat. No. CS-0148858
  • Purity≥96%
  • MDL No.None

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

4-Chloro-3-hydroxy-5-nitrobenzamide|CS-0148858

Structure of 2137975-63-2

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General Information

  • CAS No. 2137975-63-2
  • Cat. No. CS-0148858
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₅ClN₂O₄
  • Molecular Weight 216.58
  • Synonym(s) None
  • SMILES O=C(N)C1=CC([N+]([O-])=O)=C(Cl)C(O)=C1

Description

4-Chloro-3-hydroxy-5-nitrobenzamide features a trifunctional aromatic core with chlorine, hydroxyl, and nitro groups positioned for orthogonal reactivity. This electron-deficient scaffold enables direct coupling in late-stage functionalization and serves as a key intermediate in the synthesis of bioactive heterocycles under mild conditions.

Application

4-Chloro-3-hydroxy-5-nitrobenzamide serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via cyclization or nucleophilic substitution. The ortho-chloro and nitro groups facilitate downstream functionalization, while the phenolic hydroxyl offers direct derivatization potential. Its bench-stable nature and compatibility with standard coupling reactions make it suitable for multi-step synthesis workflows in API development.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS07,GHS09
Signal Word : Danger
UN#: 3077
Class : 9
Packing Group : Ⅲ
Hazard Statements : H302-H315-H317-H318-H410
Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P362+P364-P391-P501

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Computational Chemistry Data

  • TPSA   106.46
  • LogP   1.0527
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   2

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