Category: 82104-06-1

Action of Grignard reagents on halogenated phthalimides was written by El-Sharief, A. M. S.;Eid, F. A.. And the article was included in Egyptian Journal of Chemistry in 1982.Computed Properties of C15H10BrNO2 The following contents are mentioned in the article:

3-Benzalphthalimidines I (R = H, 4-Me, R¹ = 6-Br, 7-Cl; R = 2-Me, 2-OMe, 4-Cl, R¹ 6-Br) were obtained by interaction of PhCH₂MgCl with phthalimides, then dehydration of the resulting 3-benzyl-3-hydroxyphthalimidines. Interaction of PhMgBr and EtMgI with bromophthalimides is also discussed. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Computed Properties of C15H10BrNO2).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.Computed Properties of C15H10BrNO2

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

Palladium-catalyzed one-step synthesis of isoindole-1,3-diones by carbonylative cyclization of o-halobenzoates and primary amines was written by Worlikar, Shilpa A.;Larock, Richard C.. And the article was included in Journal of Organic Chemistry in 2008.Electric Literature of C15H10BrNO2 The following contents are mentioned in the article:

The palladium-catalyzed aminocarbonylation of o-halobenzoates produces 2-substituted isoindole-1,3-diones in good yields. This methodol. provides a good one-step approach to this important class of heterocycles and tolerates a variety of functional groups, including methoxy, alc., ketone, and nitro groups. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Electric Literature of C15H10BrNO2).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.Electric Literature of C15H10BrNO2

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

Oxidation of aromatic and aliphatic triisopropylsilanylsulfanyls to sulfonyl chlorides: preparation of sulfonamides was written by Gareau, Yves;Pellicelli, Jonathan;Laliberte, Sebastien;Gauvreau, Danny. And the article was included in Tetrahedron Letters in 2003.Application of 82104-06-1 The following contents are mentioned in the article:

Aromatic and aliphatic triisopropylsilanylsulfanyls were prepared and oxidized to the sulfonyl chlorides with KNO₃/SO₂Cl₂. The sulfonyl chlorides were characterized via their conversion to sulfonamides. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Application of 82104-06-1).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. Indole, first isolated in 1866, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered. 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.Application of 82104-06-1

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

Bioactive cyclometalated phthalimides: design, synthesis and kinase inhibition was written by Blanck, Sebastian;Geisselbrecht, Yann;Kraeling, Katja;Middel, Stephen;Mietke, Thomas;Harms, Klaus;Essen, Lars-Oliver;Meggers, Eric. And the article was included in Dalton Transactions in 2012.Synthetic Route of C15H10BrNO2 The following contents are mentioned in the article:

The regioselective cyclometalation of 4-(pyridin-2-yl)phthalimide was exploited for the economical design of organometallic protein kinase inhibitors. 4-(Pyridin-2-yl)phthalimide can be prepared from inexpensive 4-bromophthalimide in just three steps including one Pd-catalyzed Stille cross-coupling. The versatility of this new ligand was demonstrated with the synthesis of ruthenium(II) half-sandwich as well as octahedral ruthenium(II) and iridium(III) complexes. The regioselectivity of the C-H activation in the course of the cyclometalation can be influenced by the reaction conditions and the steric demand of the introduced metal complex fragment. The biol. activity of this new class of metalated phthalimides was evaluated by profiling two representative members against a large panel of human protein kinases. A cocrystal structure of one metallo-phthalimide with the protein kinase Pim1 confirmed an ATP-competitive binding with the intended hydrogen bonding between the phthalimide moiety and the hinge region of the ATP-binding site. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Synthetic Route of C15H10BrNO2).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Synthetic Route of C15H10BrNO2

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

Access to Multisubstituted Furan-3-carbothioates via Cascade Annulation of α-Oxo Ketene Dithioacetals with Isoindoline-1,3-dione-Derived Propargyl Alcohols was written by Bai, Li-Gang;Chen, Ming-Tao;Xiao, Dong-Rong;Zhao, Liu-Bin;Luo, Qun-Li. And the article was included in Journal of Organic Chemistry in 2018.Recommanded Product: 2-Benzyl-5-bromoisoindoline-1,3-dione The following contents are mentioned in the article:

A Bronsted acid-promoted, unprecedented formal (3 + 2) annulation strategy for the synthesis of multisubstituted furan-3-carbothioates is reported. This transformation represents the first regioselective annulation of α-oxo ketene dithio-acetals as 1,3-bis-nucleophiles in a cascade manner. The choice of isoindoline-1,3-dione-derived propargyl alcs. is crucial to the uncommon annulation mode between an alkyne-type bis-electrophile and a 1,3-bis-nucleophile under metal-free conditions. The scale-up of the synthesis and several interesting transformations of an as-synthesized product were further investigated. A Nazarov-like cyclization is proposed for the ring-closure process according to the exptl. observations. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Recommanded Product: 2-Benzyl-5-bromoisoindoline-1,3-dione).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. More than 200 indole derivatives have already been marketed as drugs or are under advanced stages of clinical trials.Recommanded Product: 2-Benzyl-5-bromoisoindoline-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

The Art of Filling Protein Pockets Efficiently with Octahedral Metal Complexes was written by Blanck, Sebastian;Maksimoska, Jasna;Baumeister, Julia;Harms, Klaus;Marmorstein, Ronen;Meggers, Eric. And the article was included in Angewandte Chemie, International Edition in 2012.Synthetic Route of C15H10BrNO2 The following contents are mentioned in the article:

The design of a metal-based enzyme inhibitor is described here. Its crystallog. anal. of its binding within enzyme active site emphasizes the broad range of possibilities for fitting octahedral metal complexes in an enzyme active site. The simplicity of the structure of complex 1 displays and IC50 value of 83nm (1μM ATP)which is superior to that of FL172, a complex that is much more tedious to synthesize and is of a higher stereochem. complexity (20 possible isomers). The ruthenium phthalimide complex 1 described here is amongst the most potent ATP-competitive inhibitors known for the protein Kinase PAK1. This demonstrates the advantage of filling large or open pockets with globular octahedral metal complexes. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Synthetic Route of C15H10BrNO2).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.Synthetic Route of C15H10BrNO2

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

Monothio- and dithiophthalimides: synthesis of dibromo-β-isoindigo and dibromodithio-β-isoindigo derivatives was written by El-Sharief, A. M. S.;Hammad, N. E.. And the article was included in Indian Journal of Chemistry in 1981.Product Details of 82104-06-1 The following contents are mentioned in the article:

5-Bromo-3-oxo-1-thioxoisoindolines and 5-bromo-1,3-dithioxoisoindolines on reaction with amines either in AcOH or under fusion give 2-aryl-1-arylimino-5-bromo-3-isoindolinones and 1-arylimino-5-bromo-3-thioxoisoindolines, resp. Dithione I on reaction with Ph₂CN₂ gives the spiro[isoindoline-thiirane] II. The 5-bromo-3-oxo-1-thioxoisoindolines and 5-bromo-1,3-dithioxoisoindolines when heated with Cu turnings in decalin give the corresponding dibromo-β-isoindigo derivatives e.g. III and dibromodithio-β-isoindigo derivs, e.g. IV. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Product Details of 82104-06-1).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Product Details of 82104-06-1

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

Application of a spin-labeled spin-trap to the detection of nitric oxide (NO) was written by Marx, Lucien;Rassat, Andre. And the article was included in Angewandte Chemie, International Edition in 2000.Safety of 2-Benzyl-5-bromoisoindoline-1,3-dione The following contents are mentioned in the article:

We suggest a new use of diradicals as spin-labeled spin-traps. These reagents would combine a stable radical (R_T), designed to trap selectively the radical to be detected and to yield diamagnetic products, and another radical (R_L), unreactive during this reaction, at a distance such that the diradical EPR spectrum would be a single line. In this way, as R_T reacts, the signal of the R_T moiety would be detected at the very beginning of the reaction, with both the concentration of spin trap and of spin adduct being monitored on the same spectrum. Furthermore, the rate of the trapping reaction (usually bimol.) could easily be increased by increasing the biradical concentration As an example of this method, we have studied the trapping of NO by a new diradical that was designed to combine two aminoxy groups on an isoindoline backbone. The diradical was prepared in six steps from phthalic anhydride. When nitric oxide was bubbled into a deoxygenated solution of the synthesized aminoxy-isoindoline derivative in ethanol, samples were taken after 10,30, 60, and 90 min and analyzed by thin layer chromatog. and EPR; a three-line spectrum, not apparent in the spectrum of the sample taken after 10 min, appeared superimposed on the diradical spectrum of the sample taken after 30 min. Four new nitroxides were then detected : they all displayed the same typical isoindolidinyloxyl(radical) 3-line EPR spectrum (toluene, a_N = 1.37 mT). This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Safety of 2-Benzyl-5-bromoisoindoline-1,3-dione).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) 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.Safety of 2-Benzyl-5-bromoisoindoline-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

Potent non-hydroxamate inhibitors of histone deacetylase-8: Role and scope of an isoindolin-2-yl linker with an α-amino amide as the zinc-binding unit was written by Greenwood, Simon O. R.;Chan, A. W. Edith;Hansen, D. Flemming;Marson, Charles M.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2020.Safety of 2-Benzyl-5-bromoisoindoline-1,3-dione The following contents are mentioned in the article:

A series of potent inhibitors of histone deacetylase-8 (HDAC8) is described that contains an α-amino amide zinc-binding unit and a substituted isoindolinyl capping group. The presence of a 2,4-dichlorophenyl unit located in the acetate-release cavity was shown to confer a gain of approx. 4.3 kJ mol^-1 in binding energy compared to a Ph group, and the isoindoline linker has approx. 5.8 kJ mol^-1 greater binding energy than the corresponding tetrahydroisoquinoline ring system. In a series of 5-substituted isoindolin-2-yl inhibitors, a 5-acetylamino derivative was found to be more potent than the 5-unsubstituted lead HDAC8 inhibitor (increase in binding energy of 2.0 kJ mol^-1, ascribed to addnl. binding interactions within the N_ε-acetyl-L-lysine binding tunnel in HDAC8, including hydrogen bonding to Asp101. Tolerance of a 5-substituent (capping group) on the isoindoline ring has been demonstrated, and which in some cases confers improved enzyme inhibition, the HDAC8 substrate-binding region providing a platform for addnl. interactions. This study involved multiple reactions and reactants, such as 2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1Safety of 2-Benzyl-5-bromoisoindoline-1,3-dione).

2-Benzyl-5-bromoisoindoline-1,3-dione (cas: 82104-06-1) belongs to indole derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. 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.Safety of 2-Benzyl-5-bromoisoindoline-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