Description
4-Chlorophthalimide (CAS No. 7147-90-2) is a high-purity organic compound with the molecular formula C8H4ClNO2. This versatile intermediate is widely used in pharmaceutical synthesis, agrochemical development, and material science research. Its unique chlorinated phthalimide structure makes it a valuable building block for heterocyclic chemistry and active pharmaceutical ingredient (API) production. Our product is rigorously tested to ensure >98% purity (HPLC) and is supplied as a fine white to off-white crystalline powder. Suitable for use in Grignard reactions, nucleophilic substitutions, and other advanced organic transformations, this compound is packaged under inert gas to ensure stability and longevity. Each batch is accompanied by comprehensive analytical data including 1H NMR, 13C NMR, and mass spectrometry reports.
Properties
- CAS Number: 7147-90-2
- Complexity: 241
- IUPAC Name: 5-chloroisoindoline-1,3-dione
- InChI: InChI=1S/C8H4ClNO2/c9-4-1-2-5-6(3-4)8(12)10-7(5)11/h1-3H,(H,10,11,12)
- InChI Key: BGJNRQSGJHVURK-UHFFFAOYSA-N
- Exact Mass: 180.9930561
- Molecular Formula: C8H4ClNO2
- Molecular Weight: 181.57
- SMILES: C1=CC2=C(C=C1Cl)C(=O)NC2=O
- Topological: 46.2
- Monoisotopic Mass: 180.9930561
- Synonyms: 4-chlorophthalimide, 5-Chloroisoindoline-1,3-dione, 7147-90-2, 5-chloroisoindole-1,3-dione, 5-chloro-2,3-dihydro-1H-isoindole-1,3-dione, MFCD08703319, 4-CHLORO-PHTHALIMIDE, NSC27008, 4-chloro phthalimide, SCHEMBL482311, SCHEMBL658064, SCHEMBL5641660, CHEMBL2252336, DTXSID40282646, BGJNRQSGJHVURK-UHFFFAOYSA-N, BDBM50487209, NSC-27008, AKOS005216105, CS-W022359, FS-3638, SB64023, SY113510
4-Chlorophthalimide serves as a key intermediate in the synthesis of bioactive compounds and pharmaceutical agents. Researchers utilize this compound in developing novel antimicrobial and antifungal derivatives through nucleophilic aromatic substitution reactions. In material science, it finds application as a precursor for advanced polymers with enhanced thermal stability. The chlorinated imide functionality enables efficient conjugation with various nucleophiles, making it valuable for medicinal chemistry programs targeting enzyme inhibition.
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