Day: December 3, 2021

Safety of 1-(4-Nitrophenyl)ethanone. Recently I am researching about 2-PHOTON ABSORPTION; OPTICAL PROPERTIES; MOLECULES; DESIGN; FLUORESCENCE; EXCITATION, Saw an article supported by the DST, INSPIRE Fellowship New Delhi, Government of India. Published in ELSEVIER in AMSTERDAM ,Authors: Saha, A; Singh, A; Chari, R; Jayabalan, J. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Using green chemical method a series of fifteen systematically substituted 3-(9-substituted anthracen-10-yl)-1-(4-phenyl substituted)prop-2-en-1-one derivatives having high nonlinear absorption coefficient have been synthesized. The nonlinear absorption properties of these compounds were studied using nanosecond pulses at 532 nm wavelength. All 15 derivatives are found to show high nonlinear absorption in the range of 35-640 cm/GW. Among these the derivatives with-NO2 as one of the substitution group show higher nonlinear absorption. The origin of high nonlinear absorption with low linear absorption in the compounds has been attributed to two-step two-photon absorption process. We have shown that the energy bands of these compounds are distributed such that for excitation at 532 nm they have strong nonlinear absorption. These properties of the reported compounds make them a potential candidate for biological imaging and other applications which are based on nonlinear absorption. (C) 2020 Elsevier B.V. All rights reserved.

Welcome to talk about 100-19-6, If you have any questions, you can contact Saha, A; Singh, A; Chari, R; Jayabalan, J or send Email.. Safety of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Coverage of Haemophilus influenzae Type b Conjugate Vaccine for Children in Mainland China Systematic Review and Meta-analysis WOS:000459304300011 published article about CHILDHOOD IMMUNIZATION; DISEASE; PREVALENCE; PNEUMONIA; SCHEDULES; PROGRAM; BURDEN in [Yang, Ya; Yang, Yu; Zhou, Yibiao; Jiang, Qingwu] Fudan Univ, Key Lab Publ Hlth Safety, Minist Educ China, Shanghai, Peoples R China; [Yang, Ya; Yang, Yu; Zhou, Yibiao; Jiang, Qingwu] Fudan Univ, Trop Dis Res Ctr, Dept Epidemiol, Sch Publ Hlth, Shanghai, Peoples R China; [Scherpbier, Robert W.; Zhu, Xu] UNICEF Beijing Off, Beijing, Peoples R China; [Chen, Yue] Univ Ottawa, Fac Med, Sch Epidemiol & Publ Hlth, Ottawa, ON, Canada in 2019.0, Cited 59.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. HPLC of Formula: C8H7NO3

Background: Use of Haemophilus influenzae type b conjugate vaccine is effective in reducing the disease burden, but its coverage in China is unclear. The aim of this meta-analysis is to assess the coverage of Hib conjugate vaccines in children in Mainland China. Methods: We systematically searched Pubmed, Web of Science, Medline, CNKI and Wanfang to identify studies assessing the coverage of Hib vaccine in Chinese children. Random-effects models were used to obtain pooled estimates for Hib vaccine coverage and analyzed heterogeneity with meta-regression and subgroup analyses. Results: Thirty-three studies that included 7,227,480 subjects in 12 provinces met our inclusion criteria. The pooled overall coverage of Hib conjugate vaccine was 54.9% [95% confidence interval (CI): 52.9-57.0]. The pooled coverage for the nonlocal population (54.3%; 95% CI: 52.4-56.3) was lower than that for the local residents (62.0%; 95% CI: 58.4-65.6). The region-pooled coverage was higher in the east of China (59.7%; 95% CI: 57.3-62.1) than in the central and west parts of the country (48.5%; 95% CI: 40.6-56.4). Overall, 26.7% (95% CI: 20.1-33.2) had 1 dose only, 14.8% (95% CI: 10.0-19.6%) had 2 doses, 13.5% (95% CI: 9.1-17.8) had 3 doses and 14.3% (95% CI: 9.7-18.9) had 4 doses. Conclusions: We found a low coverage of Hib conjugate vaccine, particularly for the nonlocal children and those living in the central and west parts of China. Including Hib vaccine into the national immunization program is recommended to reduce disparities in vaccination coverage.

Welcome to talk about 100-19-6, If you have any questions, you can contact Yang, Y; Yang, Y; Scherpbier, RW; Zhu, X; Chen, Y; Zhou, YB; Jiang, QW or send Email.. HPLC of Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Name: 2,2-Diphenylacetonitrile. Recently I am researching about CYANOBACTERIA; BIODETERIORATION; ENZYMES; COPPER; LIGHT, Saw an article supported by the Department of Research and Innovation at the University of Venda through the research incentive IP60. Published in AFRICAN CENTRE DISASTER STUDIES in POTCHEFSTROOM ,Authors: Munyai, TR; Sonqishe, T; Gumbo, JR. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile

A brick pavement, tramped by humans, is exposed to atmospheric elements, thus allowing cyanobacteria and algae to colonise. In this article, we report on the factors that contribute to the slipperiness of a brick pavement at the University of Venda in the Limpopo province of the South Africa. Samples were collected from brick surfaces either colonised by green algae (treated) or not (control). The samples were acid-digested and analysed for metals by Inductively Coupled Plasma Mass Spectrometry (ICP MS) in parts per billion (ppb). The treated bricks, with green algae, had average high metal contents (ppb): Al 9456.02, Ti 731.23, V 46.44, Cr 78.85, Mn 862.93, Fe 16295.18, Co 23.57, Ni 59.36, Cu 66.31, Zn 160.57, As 7.92, Se 10.45, Mo 6.74, Cd 5.19, Sn 4.65, Sb 2.31 and Pb 19.51. In contrast, control bricks had a low average of metal content (ppb) as follows: Al 2.99, Ti 0.28, V 4.04, Cr 1.42, Mn 4.29, Fe 20.89, Co 0.36, Ni 2.74, Cu 5.64, Zn 4.21, As 0.56, Se <3.00, Mo 0.88, Cd 0.01, Sn 1.05, Sb 0.04 and Pb 0.04. Other factors that promote algae colonisation include high solar radiation, neutral pH, nutrients, low electrical conductivity and total dissolved solids. The algae colonisation of brick pavement results in an unaesthetic sighting and a slippery surface that is hazardous to humans. Name: 2,2-Diphenylacetonitrile. Bye, fridends, I hope you can learn more about C14H11N, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article 2-Thiopyrimidine/chalcone hybrids: design, synthesis, ADMET prediction, and anticancer evaluation as STAT3/STAT5a inhibitors WOS:000521276700001 published article about OVERCOME DRUG-RESISTANCE; CHALCONE DERIVATIVES; MOLECULAR TARGETS; LEUKEMIA; CANCER; STAT3; APOPTOSIS; POTENT; DOMAIN; SRC in [Lamie, Phoebe F.; Philoppes, John N.] Beni Suef Univ, Fac Pharm, Dept Pharmaceut Organ Chem, Bani Suwayf 62514, Egypt in 2020.0, Cited 50.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. COA of Formula: C8H7NO3

A novel 2-thiopyrimidine/chalcone hybrid was designed, synthesised, and evaluated for their cytotoxic activities against three different cell lines, K-562, MCF-7, and HT-29. The most active cytotoxic derivatives were 9d, 9f, 9n, and 9p (IC50=0.77-1.74 mu M, against K-562 cell line), 9a and 9r (IC50=1.37-3.56 mu M against MCF-7 cell line), and 9a, 9l, and 9n (IC50=2.10 and 2.37 mu M against HT-29 cell line). Compounds 9a, 9d, 9f, 9n, and 9r were further evaluated for their cytotoxicity against normal fibroblast cell line WI38. Moreover, STAT3 and STAT5a inhibitory activities were determined for the most active derivatives 9a, 9d, 9f, 9n, and 9r. Dual inhibitory activity was observed in compound 9n (IC50=113.31 and 50.75 mu M, against STAT3 and STAT5a, respectively). Prediction of physicochemical properties, drug likeness score, pharmacokinetic and toxic properties was detected.

Welcome to talk about 100-19-6, If you have any questions, you can contact Lamie, PF; Philoppes, JN or send Email.. COA of Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Cu-Catalyzed one-pot synthesis of thiochromeno-quinolinone and thiochromeno-thioflavone via oxidative double hetero Michael addition using in situ generated nucleophiles WOS:000555234200022 published article about FACILE SYNTHESIS; 4-QUINOLONES; CYCLIZATION; ANNULATION; INHIBITORS; DESIGN; WATER in [Sundaravelu, Nallappan; Sekar, Govindasamy] Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India in 2020.0, Cited 41.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Product Details of 100-19-6

A copper catalyzed three-component synthesis of pi-conjugated tetracyclic thiochromeno-quinolinone and thiochromeno-thioflavone was establishedviaoxidative double hetero Michael addition usingin situgenerated nucleophiles. Xanthate plays a dual role as an odourless sulfur source and a chemoselective reducing agent. Thein situformed iodine plays a crucial role in the oxidation step.

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Sundaravelu, N; Sekar, G or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Unlocking the catalytic potential of tris(3,4,5-trifluorophenyl)borane with microwave irradiation WOS:000454919600010 published article about ASYMMETRIC HYDROBORATION; IMINE HYDROBORATION; ALKENES; ALKYNES; ISOMERIZATION; PINACOLBORANE; OVENS in [Carden, Jamie L.; Gierlichs, Lukas J.; Wass, Duncan F.; Browne, Duncan L.; Melen, Rebecca L.] Cardiff Univ, Sch Chem, Main Bldg,Pk Pl, Cardiff CF10 3AT, S Glam, Wales; [Wass, Duncan F.] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England in 2019.0, Cited 35.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Name: 1-(4-Nitrophenyl)ethanone

The catalytic activity of tris(3,4,5-trifluorophenyl)borane has been explored in the 1,2-hydroboration reactions of unsaturated sub-strates. Under conventional conditions, the borane was found to be active only in the hydroboration of aldehyde, ketone and imine substrates, with alkenes and alkynes not being reduced effectively. The use of microwave irradiation on the other hand has permitted alkenes and alkynes to be hydroborated in good yields.

Name: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Carden, JL; Gierlichs, LJ; Wass, DF; Browne, DL; Melen, RL or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Chemistry very interesting. Saw the article Enantioselective Intramolecular Allylic Substitution via Synergistic Palladium/Chiral Phosphoric Acid Catalysis: Insight into Stereoinduction through Statistical Modeling published in 2020. Formula: C14H11N, Reprint Addresses Toste, FD (corresponding author), Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA.; Sigman, MS (corresponding author), Univ Utah, Dept Chem, 315 South 1400 East, Salt Lake City, UT 84112 USA.. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile

The mode of asymmetric induction in an enantioselective intramolecular allylic substitution reaction catalyzed by a combination of palladium and a chiral phosphoric acid was investigated by a combined experimental and statistical modeling approach. Experiments to probe nonlinear effects, the reactivity of deuterium-labeled substrates, and control experiments revealed that nucleophilic attack to the pi-allylpalladium intermediate is the enantio-determining step, in which the chiral phosphate anion is involved in stereoinduction. Using multivariable linear regression analysis, we determined that multiple noncovalent interactions with the chiral environment of the phosphate anion are integral to enantiocontrol in the transition state. The synthetic protocol to form chiral pyrrolidines was further applied to the asymmetric construction of C-O bonds at fully substituted carbon centers in the synthesis of chiral 2,2-disubstituted benzomorpholines.

Welcome to talk about 86-29-3, If you have any questions, you can contact Tsai, CC; Sandford, C; Wu, T; Chen, BY; Sigman, MS; Toste, FD or send Email.. Formula: C14H11N

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Formula: C8H7NO3. I found the field of Pharmacology & Pharmacy very interesting. Saw the article Design, synthesis, and biological evaluation of chalcone-linked thiazole-imidazopyridine derivatives as anticancer agents published in 2020.0, Reprint Addresses Rao, KRM (corresponding author), Deemed Be Univ, Dept Chem, GITAM Inst Sci Gandhi Inst Technol & Management, Visakhapatnam 530045, Andhra Pradesh, India.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.

A novel library of chalcone linked thiazole-imidazopyridine (12a-j) derivatives were designed, synthesized, and their structures were characterized by(1)H NMR,C-13 NMR and mass spectral studies. Further, all compounds were tested for their anticancer effects on four human cancer cell lines including MCF-7 (breast carcinoma), A549 (lung carcinoma), DU-145 (prostate carcinoma) and MDA MB-231 (breast carcinoma) by employing MTT method, using etoposide as the positive control. Among them, compound12bdisplayed more potent anticancer activity against four cancer cell lines when compared to the positive control.

Formula: C8H7NO3. Welcome to talk about 100-19-6, If you have any questions, you can contact Suma, VR; Sreenivasulu, R; Rao, MVB; Subramanyam, M; Ahsan, MJ; Alluri, R; Rao, KRM or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Huang, RJ; Wang, YX; Liu, XX; Zhou, P; Jin, SW; Zhang, ZH in [Huang, Renjie; Wang, Yanxin; Liu, XiXi; Zhou, Peng; Jin, Shiwei; Zhang, Zehui] South Cent Univ Nationalities, Key Lab Catalysis & Mat Sci, Minist Educ, Wuhan 430074, Peoples R China published Co-N-x catalyst: an effective catalyst for the transformation of nitro compounds into azo compounds in 2021.0, Cited 24.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The selective hydrogenation of nitro compounds into their corresponding azo compounds is challenging in organic synthesis. In this study, we have developed a facile and efficient catalytic system for the transformation of nitro compounds into azo compounds under mild conditions over a heterogeneous cobalt catalyst (Co-N-x/C-800-AT). The Co-N-x/C-800-AT catalyst was found to be highly active for the reductive-coupling of nitro compounds into azo compounds in ethanol at 110 degrees C and 2.5 bar H-2 pressure with the addition of NaOH as an additive, affording structurally-diverse azo compounds with satisfactory yields (70.4-98.3%). The developed method demonstrated several advantages such as high catalytic activity and high selectivity with tolerance to other functional groups and high stability.

Category: benzodioxans. Welcome to talk about 100-19-6, If you have any questions, you can contact Huang, RJ; Wang, YX; Liu, XX; Zhou, P; Jin, SW; Zhang, ZH or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Design, synthesis, and evaluation of novel combretastatin A-4based chalcone derivatives as anticancer agents WOS:000591550900001 published article about ANTIMITOTIC NATURAL-PRODUCTS; BIOLOGICAL EVALUATION; COLCHICINE SITE; ANALOGS; TUBULIN; BINDING; CYTOTOXICITY; INHIBITION; FLAVONOIDS; MECHANISM in [Rathnakar, Bethi; Kumar, Gajula S.; Mahammad, Saleem P.; Nimma, Rameshwar; Satyanarayana, Mavurapu] Telangana Univ, Dept Pharmaceut Chem, Nizamabad, India; [Gattu, Sridhar] CSIR IICT, Organ & Biomol Div, Hyderabad, India; [Kalyani, Sambaru] Mahatma Gandhi Univ, Dept Chem & Pharmaceut Sci, Nalgonda, India in 2021.0, Cited 55.0. COA of Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A series of combretastatin A-4 based chalcones (14a-l) were designed, synthesized and these compounds examined for inhibitory effects on the proliferation of human lung (A549), breast (MCF-7), melanoma (A375), and colon (HT-29) carcinoma cells. Compounds 14b, 14c, 14e, 14h, and 14i (tri/dimethoxy, methyl, and mono/dinitro derivatives) have exhibited the most potent antiproliferative activity with IC50 < 2 mu M and the hexa methoxy derivative 14b, the most promising one, which displayed the potent inhibitory activities in MCF-7 (IC50: 10 nM), A375 (IC50: 12 nM), and A549 (IC50: 65 nM) cell lines, and is 18 times more potent than the CA-4. Compound 14b represents a new scaffold and the results provide insights into further development of anticancer agents. COA of Formula: C8H7NO3. Welcome to talk about 100-19-6, If you have any questions, you can contact Rathnakar, B; Kumar, GS; Mahammad, SP; Gattu, S; Kalyani, S; Nimma, R; Satyanarayana, M or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem