Spatz, Sydney M. et al. published their research in Industrial & Engineering Chemistry Product Research and Development in 1969 | CAS: 24407-32-7

4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Related Products of 24407-32-7

Some N-substituted tetrabromophthalimide fire-retardant additives was written by Spatz, Sydney M.;Stone, Herman. And the article was included in Industrial & Engineering Chemistry Product Research and Development in 1969.Related Products of 24407-32-7 This article mentions the following:

A broad variety of tetrabromophthalimides for screening as fire-retardant additives was prepared by reaction of tetrabromophthalic anhydride with aliphatic and aromatic amines, diamines, and hydrazines, thermolysis of di-NH4 tetrabromophthalate, and chem. transformations of tetrabromophthalimides. Preliminary tests of several imides, e.g. tetrabromophthalimide and N-(2-hydroxyethyl)phthalimide, indicate that these additives impart fire-retardancy to poly(vinyl chloride), polyester, and epoxy resins. In the experiment, the researchers used many compounds, for example, 4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7Related Products of 24407-32-7).

4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Related Products of 24407-32-7

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

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