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TCI

CAS 321-14-2

5-Chlorosalicylic Acid TCI C0287

5-Chlorosalicylic Acid TCI C0287

Chemical Identity

Other names
5-Chloro-2-hydroxybenzoic Acid · CSA
CAS No.
321-14-2
PubChem
CID 9447·SID 87565441
Formula
C7H5ClO3
Molecular weight
172.56 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
5-chloro-2-hydroxybenzoic acid
SMILES
C1=CC(=C(C=C1Cl)C(=O)O)O
InChIKey
NKBASRXWGAGQDP-UHFFFAOYSA-N
MDL
MDL00002457
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TCI C0287 5-Chlorosalicylic Acid (CAS 321-14-2) is a chlorinated salicylic acid featuring adjacent carboxyl and phenolic hydroxyl groups. This arrangement supports intramolecular hydrogen bonding and makes the compound an effective chelating ligand for transition metal ions. It is routinely used to prepare esters, amides, and other salicylate derivatives, and also serves as a linker in coordination polymer and metal–organic framework research. AMI Scientific provides this TCI building block in 25 g and 500 g packs for synthetic, coordination, and analytical chemistry laboratories.

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  • Sofia (2008). Comparative Antiphlogistic Activity of Meseclazone, 5-Chlorosalicylic Acid, Acetylsalicylic Acid, Phenylbutazone, Indomethacin and Hydrocortisone in Various Rat Paw Edema Models. Pharmacology doi:10.1159/000136760
  • Dr.Hemendra H Bhatt (2020). A Photophysical and Computational Study of 5-Chlorosalicylic Acid and Derivatives Featuring Thiadiazole, Oxadiazole, and Triazole Scaffolds. Vidhyayana doi:10.58213/9k1rtq07
  • Kök (2020). Improving of callus formation in ‘Syrah’/‘110R’ combination by 5-chlorosalicylic acid and thidiazuron treatments. Acta Horticulturae doi:10.17660/actahortic.2020.1276.14

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.