4-Chloroisatin TCI C1870

Chemical Identity

Other names: 4-Chloroindole-2,3-dione · 4-Chloro-2,3-indolinedione
CAS No.: 6344-05-4
PubChem: CID 96047·SID 87558535
Formula: C8H4ClNO2
Molecular weight: 181.58 g/mol
Purity: >97.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-chloro-1H-indole-2,3-dione
SMILES: C1=CC2=C(C(=C1)Cl)C(=O)C(=O)N2
InChIKey: HSYFISNDMZKGRS-UHFFFAOYSA-N

Rp 875.700,00

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Berat 5g 25g

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4-Chloroisatin is a chemical compound widely used in organic chemistry laboratories as a building block for the synthesis of heterocyclic compounds. Its molecular structure, featuring an aromatic ring with a chlorine substituent, makes it a versatile reagent for various chemical reactions, including substitution and ring-opening processes. This compound is commonly employed in pharmaceutical research and industrial chemistry due to its stability and reactivity. In Indonesian laboratories, it plays a crucial role in the development of new drugs and organic materials, supporting both academic and industrial research efforts. Its availability and ease of handling make it a preferred choice for researchers in the field of chemistry and pharmacology.

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(2013). Synthesis, Characterization and Biological Activities of a New 5-Chloroisatin Schiff Base and its Metal Complexes. Chemical Science Transactions doi:10.7598/cst2013.527
Pandeya et al. (2006). Synthesis and Antimicrobial Evaluation of Some 4‐ or 6‐Chloroisatin Derivatives.. ChemInform doi:10.1002/chin.200623110
Pervez et al. (2012). Synthesis and Biological Evaluation of Some New N4-Aryl Substituted 5-Chloroisatin-3-thiosemicarbazones. Medicinal Chemistry doi:10.2174/1573406411208030505

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