Hase, Y. et al. published their research in Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy in 1980 | CAS: 24407-32-7

4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7) belongs to indole derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione

The IR and Raman spectra of tetrabromophthalic anhydride, tetrabromophthalimide, N-d-tetrabromophthalimide and potassium tetrabromophthalimide was written by Hase, Y.. And the article was included in Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy in 1980.Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione This article mentions the following:

The 180-4000-cm-1 IR and 40-4000-cm-1 Raman spectra of polycrystalline tetrabromophthalic anhydride, tetrabromophthalimide and its N-deuterio derivative, and K tetrabromophthalimide were recorded and the observed frequencies assigned on the basis of C mol. symmetry. A normal coordinate anal. was carried out and the carbonyl stretching vibrations were discussed in relation to the obtained force constants In the experiment, the researchers used many compounds, for example, 4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione).

4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7) belongs to indole derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles