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Atomfair 2-Amino-6-chlorobenzoic acid C7H6ClNO2

Description 2-Amino-6-chlorobenzoic acid (CAS No. 2148-56-3) is a high-purity organic compound with the molecular formula C7H6ClNO2. This fine chemical features a benzoic acid backbone substituted with an amino group at the 2-position and a chloro group at the 6-position, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Our product is rigorously tested to ensure ??98% purity by HPLC, with controlled levels of heavy metals and residual solvents to meet stringent research standards. Available in crystalline powder form, it is packaged under inert conditions to guarantee stability and longevity. Ideal for use in combinatorial chemistry, medicinal chemistry, and as…

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Description

Description

2-Amino-6-chlorobenzoic acid (CAS No. 2148-56-3) is a high-purity organic compound with the molecular formula C7H6ClNO2. This fine chemical features a benzoic acid backbone substituted with an amino group at the 2-position and a chloro group at the 6-position, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. Our product is rigorously tested to ensure ??98% purity by HPLC, with controlled levels of heavy metals and residual solvents to meet stringent research standards. Available in crystalline powder form, it is packaged under inert conditions to guarantee stability and longevity. Ideal for use in combinatorial chemistry, medicinal chemistry, and as a building block for heterocyclic compounds.

  • CAS No: 2148-56-3
  • Molecular Formula: C7H6ClNO2
  • Molecular Weight: 171.58
  • Exact Mass: 171.0087061
  • Monoisotopic Mass: 171.0087061
  • IUPAC Name: 2-amino-6-chlorobenzoic acid
  • SMILES: C1=CC(=C(C(=C1)Cl)C(=O)O)N
  • Synonyms: 2-Amino-6-chlorobenzoic acid, 2148-56-3, Benzoic acid, 2-amino-6-chloro-, DTXSID40175761, EINECS 218-416-8

Application

2-Amino-6-chlorobenzoic acid serves as a key precursor in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other pharmacologically active molecules. Researchers utilize this compound in the development of novel benzodiazepine derivatives and as a scaffold for antimicrobial agents. Its reactive amino and carboxyl groups enable facile derivatization for structure-activity relationship studies in drug discovery programs.

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