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2-Ethoxy-6-fluorophenylboronic acid - CAS 957062-68-9

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Category
Main Product
Product Name
2-Ethoxy-6-fluorophenylboronic acid
Catalog Number
957062-68-9
Synonyms
2-Ethoxy-6-fluorophenylboronic acid
CAS Number
957062-68-9
Molecular Weight
183.97
Molecular Formula
C8H10O3BF
COA
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MSDS
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Structure
CAS 957062-68-9 2-Ethoxy-6-fluorophenylboronic acid
Specification
Purity
98%
Boiling Point
314.537ºC at 760 mmHg
Density
1.22 g/cm3
Reference Reading
1.Enhanced coagulation-photocatalytic treatment of Acid red 73 dye and real textile wastewater using UVA/synthesized MgO nanoparticles.
Jorfi S1, Barzegar G2, Ahmadi M3, Darvishi Cheshmeh Soltani R4, Alah Jafarzadeh Haghighifard N5, Takdastan A6, Saeedi R7, Abtahi M8. J Environ Manage. 2016 Apr 14;177:111-118. doi: 10.1016/j.jenvman.2016.04.005. [Epub ahead of print]
Sequencing coagulation - photocatalytic degradation using UVA/MgO nanoparticles process was investigated for Acid red 73dye removal and then treatment of a real textile wastewater. Effective operational parameters including pH and coagulant and photocatalyst dosage were studied in synthetic wastewater and then the process was applied for real wastewater. Both coagulation and photocatalytic processes were pH dependent. At coagulant dosage of 200 mg/L and initial pH of 6, the dye concentration decreased from 200 to 31 mg/L. Complete removal of AR73 was observed with MgO nanoparticles of 0.8 g/L, initial pH of 5 and reaction time of 60 min. Langmuir-Hinshelwood model was well fitted with removal results (R2: 0.939-0.988 for different initial dye concentration). In the case of real textile wastewater, the sequence coagulation-UVA/MgO nanoparticles photocatalytic degradation yielded considerable total COD and TOC removal 98.3% and 86.9%respectively, after 300 min.
2.Accelerating full thickness wound healing using Collagen Sponge of Mrigal Fish (Cirrhinus cirrhosus) scale Origin.
Pal P1, Srivas PK1, Dadhich P1, Das B1, Maity PP1, Moulik D2, Dhara S3. Int J Biol Macromol. 2016 Apr 13. pii: S0141-8130(16)30340-3. doi: 10.1016/j.ijbiomac.2016.04.032. [Epub ahead of print]
The potentiality of collagen sponge as a skin substitute, derived from mrigal (Cirrhinus cirrhosus) scale has been explored in this study. Acid soluble collagen (ASC) and pepsin soluble collagen (PSC) from the scale of mrigal were isolated and characterized. The yields of ASC and PSC were ∼3% and ∼7% based on the dry weight of scale while the hydroxyproline content was ∼90mg/g. Scanning electron microscope revealed progressive demineralization with EDTA on time dependent scale. Further, the D-Spacing in fibril bundles were calculated to be ∼67nm. Fourier transform infrared and circular dichroism spectra confirmed extracted protein to be collagen I, where both ASC and PSC comprised of two different α-chains (α1 and α2). The denaturation temperature (Td) of the collagen solution was 35°C closer to Td of mammalian collagen. In vitro cell culture studies on the extracted collagen sponge showed efficient cell growth and proliferation. Additionally, co-culture with fibroblast and keratinocyte cells showed development of stratified epidermal layer in vitro.
3.Clinical Drug-Drug Pharmacokinetic Interaction Potential of Sucralfate with Other Drugs: Review and Perspectives.
Sulochana SP1, Syed M2, Chandrasekar DV1, Mullangi R1, Srinivas NR3. Eur J Drug Metab Pharmacokinet. 2016 Apr 16. [Epub ahead of print]
Sucralfate, a complex of aluminium hydroxide with sulfated sucrose, forms a strong gastrointestinal tract (GIT) mucosal barrier with excellent anti-ulcer property. Because sucralfate does not undergo any significant oral absorption, sucralfate resides in the GIT for a considerable length of time. The unabsorbed sucralfate may alter the pharmacokinetics of the oral drugs by impeding its absorption and reducing the oral bioavailability. Because of the increased use of sucralfate, it was important to provide a reappraisal of the published clinical drug-drug interaction studies of sucralfate with scores of drugs. This review covers several category of drugs such as non-steroidal anti-inflammatory drugs, fluoroquinolones, histamine H2-receptor blockers, macrolides, anti-fungals, anti-diabetics, salicylic acid derivatives, steroidal anti-inflammatory drugs and provides pharmacokinetic data summary along with study design, objectives and key remarks.
4.Influence of Mining Pollution on Metal Bioaccumulation and Biomarker Responses in Cave Dwelling Fish, Clarias gariepinus.
du Preez G1, Wepener V2. Bull Environ Contam Toxicol. 2016 Apr 16. [Epub ahead of print]
Cave ecosystems remain largely unstudied and risk being severely degraded as a result of anthropogenic activities. The Wonderfontein Cave, situated in the extensive gold mining region of the Witwatersrand Basin, is one such system that hosts a population of Clarias gariepinus, which is exposed to the influx of polluted mine water from the Wonderfontein Spruit River. The aim of this study was to investigate the bioaccumulation of metals, as well as relevant biomarkers, in C. gariepinus specimens sampled from the Wonderfontein Cave during high (April 2013) and low (September 2013) flow surveys. Results were also compared to a surface population associated with the Wonderfontein Spruit River. There were temporal differences in metal bioaccumulation patterns and this was attributed to the lack of dilution during the low flow period. Metals associated with acid mine drainage, i.e. Co, Mn and Zn were significantly higher in the Wonderfontein Cave population and were reflected in an increase in oxidative stress biomarkers (catalase, protein carbonyls and superoxide dismutase) and the induction of metallothionein, a biomarker of metal exposure.
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