Category: 53784-83-1

Synthesis of glycopolymer nanosponges with enhanced adsorption performances for boron removal and water treatment was written by Liao, Xueping;Wang, Bingyu;Zhang, Qiang. And the article was included in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2018.Safety of Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin This article mentions the following:

The high-affinity interactions between cis-diols and boric/boronic acid have been widely used as a tool for carbohydrate anal., protein separation and B removal. Here, we report the design and synthesis of cyclodextrin-scaffolded glycopolymers as bifunctional nanosponges for B removal and water treatment for the 1st time. Different glycopolymer nanosponges (GNs) were synthesized from monosaccharides and 尾-cyclodextrin via a combination of a crosslinking reaction, Fischer glycosylation and a click reaction. Such functional GNs are mesoporous polymer frameworks with cis-diol-containing saccharides immobilized on the surface, which have exhibited selective adsorption behavior towards boric acid depending on the structure of the GNs and the loaded saccharides. The GNs showed remarkable adsorption rates and capacities for an organic dye as a model pollutant in this work. Secondary bonding, such as H bonding and van der Waals forces between the immobilized saccharides and the adsorbates is believed to be responsible for the significantly enhanced adsorption rates and capacities. Such bifunctional materials may exhibit potential applications in seawater desalination and water treatment. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin (cas: 53784-83-1Safety of Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin).

Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Safety of Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

The hemolytic properties of chemically modified cyclodextrins was written by Bost, Mireille;Laine, Valerie;Pilard, Florence;Gadelle, Andree;Defaye, Jacques;Perly, Bruno. And the article was included in Journal of Inclusion Phenomena and Molecular Recognition in Chemistry in 1997.Safety of Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin This article mentions the following:

The hemolytic properties of natural cyclodextrins, especially of the more common cyclomaltoheptaose entity, severely hamper their potential use as carriers in pharmaceutical applications where parenteral administration is concerned. A systematic investigation on the role of chem. modifications with regard to the hemolytic character was carried out involving C-6 branched neutral, anionic, cationic and amphoteric derivatives From these data, conclusions have been drawn about the charge and the geometry of the modification: (1) substitution at primary hydroxyl groups usually decreases the hemolytic character and the geometry of the substituent affects the hemolytic property; (2) introduction of an amino group, resulting in a pos. charge at physiol. pH, decreases the hemolytic character; (3) neg. charges are comparatively less effective in reducing the hemolytic character; (4) zwitterionic groups seem to enhance the hemolytic character of the cyclodextrin mol. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin (cas: 53784-83-1Safety of Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin).

Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Safety of Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Mannosylated Poly(ethylene imine) Copolymers Enhance saRNA Uptake and Expression in Human Skin Explants was written by Blakney, Anna K.;Abdouni, Yamin;Yilmaz, Gokhan;Liu, Renjie;McKay, Paul F.;Bouton, Clement R.;Shattock, Robin J.;Becer, C. Remzi. And the article was included in Biomacromolecules in 2020.Electric Literature of C42H63Br7O28 This article mentions the following:

MRNA is a promising platform for both vaccines and therapeutics, and self-amplifying RNA (saRNA) is particularly advantageous, as it enables higher protein expression and dose minimization. Here, we present a delivery platform for targeted delivery of saRNA using mannosylated poly(ethylene imine) (PEI) enabled by the host-guest interaction between cyclodextrin and adamantane. We show that the host-guest complexation does not interfere with the electrostatic interaction with saRNA and observed that increasing the degree of mannosylation inhibited transfection efficiency in vitro, but enhanced the number of cells expressing GFP by 8-fold in human skin explants. Besides, increasing the ratio of glycopolymer to saRNA also enhanced the percentage of transfected cells ex vivo. We identified that these mannosylated PEIs specifically increased protein expression in the epithelial cells resident in human skin in a mannose-dependent manner. This platform is promising for further study of glycosylation of PEI and targeted saRNA delivery. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin (cas: 53784-83-1Electric Literature of C42H63Br7O28).

Heptakis(6-Bromo-6-Deoxy)-尾-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.Electric Literature of C42H63Br7O28

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Per-halogenation of primary hydroxy groups of β-cyclodextrin was written by Aoki, Nobuyoshi;Hattori, Kenjiro. And the article was included in Kenkyu Hokoku – Kanagawa-ken Sangyo Gijutsu Sogo Kenkyusho in 2005.HPLC of Formula: 53784-83-1 This article mentions the following:

Per-halogenation of primary hydroxyl groups of β-cyclodextrin (β-CD) was investigated as an important way for the regioselective modification of β-CD. The high regioselectivity in the halogenation was discussed in terms of the reactivity to the S_N2 reaction at each position on the anhydroglucopyranose unit. The reaction using halogenating reagent, such as, methanesulfonyl chloride, thionyl chloride, and thionyl bromide, yielded the corresponding per-6-chloro-per-6-deoxy-β-CD (80 and 90% yield) or per-6-bromo-per-6-deoxy-β-CD (70% yield) after several hours. The obtained product was halogenated only at C-6 and the halogenation at a secondary position was not observed The reactivity at C-3 of β-CD was lower than the corresponding reaction of other saccharides, such as cellulose. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1HPLC of Formula: 53784-83-1).

Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Most of the natural organobromine compounds are produced by marine organisms, and several brominated metabolites with antibacterial, antitumor, antiviral, and antifungal activity have been isolated from seaweed, sponges, corals, molluscs, and others. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.HPLC of Formula: 53784-83-1

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Synthesis of glycopolymer nanosponges with enhanced adsorption performances for boron removal and water treatment was written by Liao, Xueping;Wang, Bingyu;Zhang, Qiang. And the article was included in Journal of Materials Chemistry A: Materials for Energy and Sustainability in 2018.Safety of Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin This article mentions the following:

The high-affinity interactions between cis-diols and boric/boronic acid have been widely used as a tool for carbohydrate anal., protein separation and B removal. Here, we report the design and synthesis of cyclodextrin-scaffolded glycopolymers as bifunctional nanosponges for B removal and water treatment for the 1st time. Different glycopolymer nanosponges (GNs) were synthesized from monosaccharides and β-cyclodextrin via a combination of a crosslinking reaction, Fischer glycosylation and a click reaction. Such functional GNs are mesoporous polymer frameworks with cis-diol-containing saccharides immobilized on the surface, which have exhibited selective adsorption behavior towards boric acid depending on the structure of the GNs and the loaded saccharides. The GNs showed remarkable adsorption rates and capacities for an organic dye as a model pollutant in this work. Secondary bonding, such as H bonding and van der Waals forces between the immobilized saccharides and the adsorbates is believed to be responsible for the significantly enhanced adsorption rates and capacities. Such bifunctional materials may exhibit potential applications in seawater desalination and water treatment. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1Safety of Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin).

Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Safety of Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

The hemolytic properties of chemically modified cyclodextrins was written by Bost, Mireille;Laine, Valerie;Pilard, Florence;Gadelle, Andree;Defaye, Jacques;Perly, Bruno. And the article was included in Journal of Inclusion Phenomena and Molecular Recognition in Chemistry in 1997.Safety of Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin This article mentions the following:

The hemolytic properties of natural cyclodextrins, especially of the more common cyclomaltoheptaose entity, severely hamper their potential use as carriers in pharmaceutical applications where parenteral administration is concerned. A systematic investigation on the role of chem. modifications with regard to the hemolytic character was carried out involving C-6 branched neutral, anionic, cationic and amphoteric derivatives From these data, conclusions have been drawn about the charge and the geometry of the modification: (1) substitution at primary hydroxyl groups usually decreases the hemolytic character and the geometry of the substituent affects the hemolytic property; (2) introduction of an amino group, resulting in a pos. charge at physiol. pH, decreases the hemolytic character; (3) neg. charges are comparatively less effective in reducing the hemolytic character; (4) zwitterionic groups seem to enhance the hemolytic character of the cyclodextrin mol. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1Safety of Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin).

Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Safety of Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Mannosylated Poly(ethylene imine) Copolymers Enhance saRNA Uptake and Expression in Human Skin Explants was written by Blakney, Anna K.;Abdouni, Yamin;Yilmaz, Gokhan;Liu, Renjie;McKay, Paul F.;Bouton, Clement R.;Shattock, Robin J.;Becer, C. Remzi. And the article was included in Biomacromolecules in 2020.Electric Literature of C42H63Br7O28 This article mentions the following:

MRNA is a promising platform for both vaccines and therapeutics, and self-amplifying RNA (saRNA) is particularly advantageous, as it enables higher protein expression and dose minimization. Here, we present a delivery platform for targeted delivery of saRNA using mannosylated poly(ethylene imine) (PEI) enabled by the host-guest interaction between cyclodextrin and adamantane. We show that the host-guest complexation does not interfere with the electrostatic interaction with saRNA and observed that increasing the degree of mannosylation inhibited transfection efficiency in vitro, but enhanced the number of cells expressing GFP by 8-fold in human skin explants. Besides, increasing the ratio of glycopolymer to saRNA also enhanced the percentage of transfected cells ex vivo. We identified that these mannosylated PEIs specifically increased protein expression in the epithelial cells resident in human skin in a mannose-dependent manner. This platform is promising for further study of glycosylation of PEI and targeted saRNA delivery. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1Electric Literature of C42H63Br7O28).

Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromo compounds are employed in a variety of metal-catalyzed coupling reactions. They are also ideal candidates for the synthesis of Grignard reagents that have wide-applicability in organic synthesis. alpha-Bromoesters are employed in the Reformatsky reaction for the synthesis of beta-hydroxyesters. When the molecular ion is detected, the bromine and chlorine isotope patterns are very distinct, but caution is to be exercised for certain mixed chlorinated/brominated compounds, which can look similar to homohalogen patterns.Electric Literature of C42H63Br7O28

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Improved synthesis of 6-deoxy analogs of cyclodextrins and amylose. Further interpretations of the proton magnetic resonance spectra of the peracetates of cyclodextrins and amylose was written by Takeo, Ken’ichi;Sumimoto, Tatsuo;Kuge, Takashi. And the article was included in Staerke in 1974.Synthetic Route of C42H63Br7O28 This article mentions the following:

Reaction of cyclohexa-, -hepta-, and octa-amyloses and amylose with MeSO2Br gave the 6-bromo-6-deoxy derivatives, which were converted with Ac2O into the 2,3-di-O-acetyl-6-bromo-6-deoxy derivatives Reductive debromination of the latter with NaBH4 in Me2SO gave the 2,3-di-O-acetyl-6-deoxy derivatives, which were deacetylated to give the6-deoxy derivatives The purity and structure of the prepared compounds were confirmed by identification of the methanolysis products by chromatog. and PMR spectra. The 6-deoxy derivatives of α-, β-, and γ-cyclodextrin and amylose were composed of 95, 97, 94, and 92% 6-deoxy-D-glucose, resp. The conformation of the 2,3-di-O-acetyl-6-bromo-6-deoxy and 2,3-di-O-acetyl-6-deoxy derivatives of the cyclodextrins and amylose was investigated by PMR spectroscopy. The chem. shift changes due to the modification at C-6 were studied for the Me protons of the ring and Ac group. In the experiment, the researchers used many compounds, for example, Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1Synthetic Route of C42H63Br7O28).

Heptakis(6-Bromo-6-Deoxy)-β-Cyclodextrin (cas: 53784-83-1) belongs to organobromine compounds. Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents. Bromine-containing agents predominate because not only are they more efficient than similar chlorine-containing species, but also the high atomic weight of bromine ensures that it is present in a high mass fraction within most organobromine compounds.Synthetic Route of C42H63Br7O28

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary