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CS-W001157 4
Total: USD 88.00

2-Amino-3,5-dichlorobenzoic acid

  • CAS No. 2789-92-6

  • Cat. No. CS-W015354
  • Purity≥96%
  • MDL No.MFCD00017088

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

2-Amino-3,5-dichlorobenzoic acid|CS-W015354

Structure of 2789-92-6

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General Information

  • CAS No. 2789-92-6
  • Cat. No. CS-W015354
  • Purity ≥96%
  • MDL No. MFCD00017088
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₅Cl₂NO₂
  • Molecular Weight 206.02
  • Synonym(s) Benzoic acid, 2-amino-3,5-dichloro- (9CI)
  • SMILES O=C(O)C1=CC(Cl)=CC(Cl)=C1N

Description

2-Amino-3,5-dichlorobenzoic acid features a sterically hindered aromatic core with complementary electron-withdrawing chloro groups and a reactive amino functionality. This combination enables direct coupling in peptide synthesis and facilitates conjugation to polymer backbones or biomolecules under mild conditions. The carboxylic acid group provides solubility in polar media and serves as a handle for amide bond formation.

Application

2-Amino-3,5-dichlorobenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its ortho-amino and carboxylic acid functionalities provide orthogonal reactivity for amide coupling, cyclization, and electrophilic substitution reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in API development.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   63.32
  • LogP   2.2738
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   1

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