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9,10-Dibromoanthracene-2-sulfonyl chloride - CAS 210174-74-6

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Category
Main Product
Product Name
9,10-Dibromoanthracene-2-sulfonyl chloride
Catalog Number
210174-74-6
Synonyms
9,10-dibromoanthracene-2-sulfonylchloride;9,10-dibromoanthracene-2-sulfonylChloride;210174-74-6;AC1NED20;CTK1A0010;ZINC72399675
CAS Number
210174-74-6
Molecular Weight
434.53
Molecular Formula
C14H7Br2ClO2S
COA
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MSDS
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Canonical SMILES
C1=CC=C2C(=C1)C(=C3C=CC(=CC3=C2Br)S(=O)(=O)Cl)Br
InChI
InChI=1S/C14H7Br2ClO2S/c15-13-9-3-1-2-4-10(9)14(16)12-7-8(20(17,18)19)5-6-11(12)13/h1-7H
InChIKey
AZFXTUUUGCMHGD-UHFFFAOYSA-N
Structure
CAS 210174-74-6 9,10-Dibromoanthracene-2-sulfonyl chloride
Specification
Purity
95%
Boiling Point
544.6ºC at 760 mmHg
Density
1.916g/cm3
Appearance
Bright Yellow Solid
Reference Reading
1.Hydroxyapatite nanoparticles: preparation, characterization, and evaluation of their potential use in bone targeting: an animal study.
Maia AL1, Cavalcante CH, Souza MG, Ferreira CA, Rubello D, Chondrogiannis S, Cardoso VN, Ramaldes GA, Barros AL, Soares DC. Nucl Med Commun. 2016 Apr 12. [Epub ahead of print]
OBJECTIVE: Hydroxyapatite is used as a drug-delivery system for bone therapy applications because of its biocompatibility, bioactivity, and osteoconductive properties. In addition, hydroxyapatite nanoparticles (HApN) might be used as a theranostic probe. The aim of this study was to prepare and characterize hydroxyapatite mesoporous nanoparticles, and radiolabel these nanoparticles with technetium-99m (Tc). Moreover, biodistribution studies were carried out in healthy mice.
2.Functional lateralization of the medial prefrontal cortex in the modulation of anxiety in mice: Left or right?
Costa NS1, Vicente MA2, Cipriano AC1, Miguel TT3, Nunes-de-Souza RL4. Neuropharmacology. 2016 Apr 11. pii: S0028-3908(16)30147-2. doi: 10.1016/j.neuropharm.2016.04.011. [Epub ahead of print]
It has been suggested that the left medial prefrontal cortex (LmPFC) has an inhibitory role in controlling the right mPFC (RmPFC), thereby reducing the deleterious effects of stressors on emotional states. Here, we investigated the effects on anxiety of bilateral or unilateral injections of NOC-9 [a nitric oxide (NO) donor] and cobalt chloride (CoCl2; a synaptic inhibitor) into the mPFC of mice exposed to the elevated plus-maze (Experiments 1 and 2). The effects of restraint or social defeat on anxiety in undrugged mice were recorded at 5 minutes or 24 hours after exposure to the stress (Experiment 3). Experiment 4 investigated the effects of LmPFC injection of CoCl2 combined with restraint or social defeat on anxiety, which was recorded 24 h later. Although intra-RmPFC NOC-9 produced anxiogenesis, its injection into the LmPFC, or bilaterally, did not change anxiety. Intra-RmPFC or -LmPFC injection of CoCl2 produced anxiolytic- and anxiogenic-like effects, respectively.
3.In vivo immunomodulatory effects of plant flavonoids in lipopolysaccharide-challenged broilers.
Kamboh AA1, Hang SQ1, Khan MA2, Zhu WY1. Animal. 2016 Apr 15:1-7. [Epub ahead of print]
Plant flavonoids are generally regarded as natural replacers of synthetic growth promoters in poultry production. This study investigated the immunomodulatory effects of plant flavonoids, such as genistein and hesperidin, in lipopolysaccharide (LPS)-challenged broilers. A total of 700 21-day-old commercial Arbor Acres broiler chicks were randomly assigned into six treatment groups, each having six pens of 20 chicks/pen. Chicks were fed a basal diet without any additive (control, CON), 5 mg genistein/kg feed (G5), 20 mg hesperidin/kg (H20), or a basal diet with a combination of genistein and hesperidin (1 : 4) with doses of 5 mg/kg feed (GH5), 10 mg/kg (GH10) and 20 mg/kg (GH20) for 6 weeks. Half of the birds from each treatment were separated, and either challenged with 0·9% sodium chloride solution or Escherichia coli LPS (250 μg/kg BW) on days 16, 18 and 20. The results showed that both genistein and hesperidin improved (P<0.01) the plasma antioxidant status of growing broilers, by increasing total antioxidant capacity (TAOC), superoxide dismutase (SOD) activity and decreasing malondialdehyde production.
4.Hypocalcemia in trauma patients receiving massive transfusion.
Giancarelli A1, Birrer KL2, Alban RF3, Hobbs BP2, Liu-DeRyke X4. J Surg Res. 2016 May 1;202(1):182-7. doi: 10.1016/j.jss.2015.12.036. Epub 2015 Dec 30.
BACKGROUND: Massive transfusion protocol (MTP) is increasingly used in civilian trauma resuscitation. Calcium is vital for coagulation, but hypocalcemia commonly occurs during massive transfusion due to citrate and serum calcium chelation. This study was conducted to determine the incidence of hypocalcemia and severe hypocalcemia in trauma patients who receive massive transfusion and to compare characteristics of patients with severe versus nonsevere hypocalcemia.
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