Month: November 2021

An article The aqueous solubility of common organic groundwater contaminants as a function of temperature between 5 and 70 degrees C WOS:000456223500020 published article about THERMAL-ENERGY STORAGE; POLYCYCLIC AROMATIC-HYDROCARBONS; WATER; DEPENDENCE; LIQUIDS; CHLOROBENZENES; COEFFICIENTS; DISSOLUTION; MOBILITY; BENZENE in [Koproch, Nicolas; Dahmke, Andreas; Koeber, Ralf] Univ Kiel, Appl Geosci, Ludewig Meyn Str 10, D-24118 Kiel, Germany in 2019.0, Cited 42.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Category: chlorides-buliding-blocks

High-temperature thermal energy storage in shallow aquifers can potentially increase ambient groundwater temperatures up to 70 degrees C or even more. Since an increase in temperature is expected to influence contaminant mass flux into groundwater monitoring the spreading of organic contaminants located in the subsurface is crucial. In numerous former studies, the NAPL solubility, one major parameter controlling mass flux on field scale, was measured at temperatures up to 70 degrees C for a broad spectrum of organic substances. However, quantitative calculations of solubilities as a function of temperature considering a compiled database are largely missing. Aiming to examine the reliability of existing solubility-temperature relationships, to describe them functionally and further to identify knowledge gaps, previously published data on solubilities of 42 different organic groundwater contaminants were evaluated in this study. By using a common temperature regression function, the calculated solubility curves from compiled solubility data for 5-70 degrees C show relative changes between a few percent (CHCs and BTEX) and up to 2000% (PAH5). As published temperature-dependent solubilities for chlorinated ethylenes are contradictory in parts, solubilities of tetrachloroethylene, trichloroethylene, 1,2-cis-dichloroethylene and 1,2-trans-dichloroethylene were additionally investigated in more detail using batch experiments between 5 and 70 degrees C. The results show distinctive solubility minima at medium temperatures (20-40 degrees C) with concentrations decreasing from 5 degrees C to the minimum by 10-20%. The measured and calculated temperature-dependent solubilities enable a more reliable assessment of thermal energy storage at contaminated sites, of existing thermal remediation approaches and of combinations of underground heat storage with groundwater remediation. (C) 2018 Elsevier Ltd. All rights reserved.

Category: chlorides-buliding-blocks. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Koproch, N; Dahmke, A; Kober, R or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Ye, TY; Han, YF; Wang, RX; Yan, PZ; Chen, SW; Hou, YL; Zhao, YF in [Ye, Tianyu; Han, Yufei; Wang, Ruxin; Yan, Pingzhen; Chen, Shaowei; Hou, Yunlei; Zhao, Yanfang] Shenyang Pharmaceut Univ, Sch Pharmaceut Engn, 103 Wenhua Rd, Shenyang 110016, Peoples R China published Design, synthesis and biological evaluation of novel 2,4-bismorpholinothieno[3,2-d ]pyrimidine and 2-morpholinothieno[3,2-d] pyrimidinone derivatives as potent antitumor agents in 2020, Cited 30. HPLC of Formula: C7H8ClN. The Name is 2-Chloro-6-methylaniline. Through research, I have a further understanding and discovery of 87-63-8.

To develop novel therapeutic agents with anticancer activities, two series of novel 2,4-bismorpholinyl-thieno [3,2-d]pyrimidine and 2-morpholinothieno[3,2-d]pyrimidinone derivatives were designed, synthesized and evaluated for their biological activities. Among them, compound A(12) showed the most potent antitumor activities against HCT116, PC-3, MCF-7, A549 and MDA-MB-231 cell lines with IC50 values of 3.24 mu M, 14.37 mu M, 7.39 mu M, 7.10 mu M, and 16.85 mu M, respectively. Further explorations in bioactivity were conducted to clarify the anticancer mechanism of compound A(12). The results showed that compound A(12) obviously inhibited the proliferation of A549 cell lines and decreased mitochondrial membrane potential, which led to the apoptosis of cancer cells and suppressed the migration of tumor cells.

Welcome to talk about 87-63-8, If you have any questions, you can contact Ye, TY; Han, YF; Wang, RX; Yan, PZ; Chen, SW; Hou, YL; Zhao, YF or send Email.. HPLC of Formula: C7H8ClN

Reference:
Patent; ASTRAZENECA AB; NPS PHARMACEUTICALS, INC.; WO2006/20879; (2006); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

In 2020 ACS CATAL published article about HYDROGEN-EXCHANGE; AROMATIC-AMINES; SUBSTITUTED DIALKYLANILINES; ALKYLATION; ACTIVATION; MECHANISM; ACID in [Colomer, Ignacio] Univ Autonoma Madrid, Dept Organ Chem, Madrid 28049, Spain; [Colomer, Ignacio] IMDEA Nanociencia, Madrid 28049, Spain in 2020, Cited 65. The Name is 2-Chloro-6-methylaniline. Through research, I have a further understanding and discovery of 87-63-8. SDS of cas: 87-63-8

Providing new methods for the selective functionalization of small molecules is highly desirable, because installing molecular diversity in a desired position, for example, allows one to modulate bioactive molecules. This work reports a method for the selective functionalization of anilines using hexafluoroisopropanol (HFIP) as a solvent to promote an acid-catalyzed hydroarylation of olefins. Mechanistic experiments revealed that HFIP both protonates the alkene and selectively enables anilines toward the electrophilic aromatic substitution. This powerful strategy has been applied to the functionalization of the anti-inflammatory mefenamic acid with chemocontrol and regiocontrol.

SDS of cas: 87-63-8. Welcome to talk about 87-63-8, If you have any questions, you can contact Colomer, I or send Email.

Reference:
Patent; ASTRAZENECA AB; NPS PHARMACEUTICALS, INC.; WO2006/20879; (2006); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Recommanded Product: 2,4-Dichlorobenzoic acid. Taha, M; Uddin, N; Ali, M; Anouar, E; Rahim, F; Khan, G; Farooq, RK; Gollapalli, M; Iqbal, N; Farooq, M; Khan, KM in [Taha, Muhammad] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat IRMC, Dept Clin Pharm, POB 1982, Dammam 31441, Saudi Arabia; [Uddin, Nizam] Univ Karachi, Dept Chem, Karachi 75270, Pakistan; [Ali, Muhammad] Univ Nizwa, Nat & Med Sci Res Ctr, POB 33, Birkat Al Mauz 616, Nizwa, Oman; [Anouar, El Hassane] Prince Sattam bin Abdulaziz Univ, Coll Sci & Humanities Al Kharj, Dept Chem, Al Kharj 11942, Saudi Arabia; [Rahim, Fazal] Hazara Univ, Dept Chem, Mansehra 21300, Khyber Pakhtunk, Pakistan; [Khan, Gulraiz] Imam Abdulrahman Bin Faisal Univ, Environm Engn Dept, Coll Engn Bldg A13,POB 1982, Dammam 31441, Saudi Arabia; [Farooq, Rai Khalid] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat IRMC, Dept Neurosci Res, POB 1982, Dammam 31441, Saudi Arabia; [Gollapalli, Mohammed] Imam Abdulrahman Bin Faisal Univ, Coll Comp Sci & Informat Technol CCSIT, Dept Comp Informat Syst, POB 1982, Dammam 31441, Saudi Arabia; [Iqbal, Naveed] Univ Poonch Rawalakot AJK, Dept Chem, Rawalakot, Pakistan; [Farooq, Muhammad] Hazara Univ, Dept Phys, Mansehra 21300, Khyber Pakhtunk, Pakistan; [Khan, Khalid Mohammed] Univ Karachi, Int Ctr Chem & Biol Sci, HEJ Res Inst Chem, Karachi 75270, Pakistan published Inhibition potential of phenyl linked benzimidazole-triazolothiadiazole modular hybrids against beta-glucuronidase and their interactions thereof in 2020, Cited 54. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0.

beta-Glucuronidase is responsible for the catalytic deconjugation of beta-D-glucuronides. beta-Glucuronidase has evolved to be a viable molecular target for numerous therapeutic treatments. It plays a pivotal role in the metabolism of drugs and endogenous substances. Herein, we report the inhibitory potentials of newly developed and modular benzimidazole-triazolothiadiazole hybrids spaced through a phenyl linker (1-26) and their interactions with the beta-glucuronidase. All analogues showed IC50 values in the range of 1.30 +/- 0.10 to 44.10 +/- 0.80 mu M, and hence were found to have outstanding inhibitory potential as compare to the standard D-saccharic acid 1,4-lactone (IC50 = 48.4 +/- 1.25 mu M). These modular hybrids were successfully synthesized, rigorously characterized through various spectroscopic techniques. Molecular docking studies further revealed the potential interactions between the inhibitor and active amino acid site in beta-glucuronidase. These findings helped in identifying the potential for new drug candidates. A Plausible structure activity relationship (SAR) were established which suggested that variation in the inhibitory potential was mainly based upon the substituents attached to the phenyl ring. (C) 2020 Elsevier B.V. All rights reserved.

Bye, fridends, I hope you can learn more about C7H4Cl2O2, If you have any questions, you can browse other blog as well. See you lster.. Recommanded Product: 2,4-Dichlorobenzoic acid

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Recently I am researching about BIOLOGICAL EVALUATION; DERIVATIVES; ANTIMALARIAL; OXADIAZOLE; PYRAZOLE; DESIGN, Saw an article supported by the University Grants Commission, New DelhiUniversity Grants Commission, India. Application In Synthesis of 2,6-Dichlorobenzoic acid. Published in ACADEMIC PRESS INC ELSEVIER SCIENCE in SAN DIEGO ,Authors: Verma, G; Khan, MF; Nainwal, LM; Ishaq, M; Akhter, M; Bakht, A; Anwer, T; Afrin, F; Islamuddin, M; Husain, I; Alam, MM; Shaquiquzzaman, M. The CAS is 50-30-6. Through research, I have a further understanding and discovery of 2,6-Dichlorobenzoic acid

In continuance with earlier reported work, an extension has been carried out by the same research group. Mulling over the ongoing condition of resistance to existing antimalarial agents, we had reported synthesis and antimalarial activity of certain pyrazole-1,3,4-oxadiazole hybrid compounds. Bearing previous results in mind, our research group ideated to design and synthesize some more derivatives with varied substitutions of acetophenone and hydrazide. Following this, derivatives 5a-r were synthesized and tested for antimalarial efficacy by schizont maturation inhibition assay. Further, depending on the literature support and results of our previous series, certain potent compounds (5f, 5n and 5r) were subjected to Falcipain-2 inhibitory assay. Results obtained for these particular compounds further strengthened our hypothesis. Here, in this series, compound 5f having unsubstituted acetophenone part and a furan moiety linked to oxadiazole ring emerged as the most potent compound and results were found to be comparable to that of the most potent compound (indole bearing) of previous series. Additionally, depending on the available literature, compounds (5a-r) were tested for their antileishmanial potential. Compounds 5a, 5c and 5r demonstrated dose-dependent killing of the promastigotes. Their IC50 values were found to be 33.3 +/- 1.68, 40.1 +/- 1.0 and 19.0 +/- 1.47 mu g/mL respectively. These compounds (5a, 5c and 5r) also had effects on amastigote infectivity with IC50 of 44.2 +/- 2.72, 66.8 +/- 2.05 and 73.1 +/- 1.69 mu g/mL respectively. Further target validation was done using molecular docking studies. Acute oral toxicity studies for most active compounds were also performed.

Application In Synthesis of 2,6-Dichlorobenzoic acid. Welcome to talk about 50-30-6, If you have any questions, you can contact Verma, G; Khan, MF; Nainwal, LM; Ishaq, M; Akhter, M; Bakht, A; Anwer, T; Afrin, F; Islamuddin, M; Husain, I; Alam, MM; Shaquiquzzaman, M or send Email.

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Recommanded Product: 50-84-0. Qian, BF; Wang, JL; Jia, AQ; Shi, HT; Zhang, QF in [Qian, Bing-Feng; Wang, Jun-Ling; Jia, Ai-Quan; Shi, Hua-Tian; Zhang, Qian-Feng] Anhui Univ Technol, Inst Mol Engn & Appl Chem, Maanshan 243002, Anhui, Peoples R China published New (mu-oxo)bis(mu-carboxylato)diruthenium(III) complexes containing 1,4,7-trimethyl-1,4,7-triazacyclononane ligands in 2021, Cited 24. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0.

Treatment of [(Me3tacn)RuCl3 center dot H2O] (Me3tacn = 1,4,7-trimethyl-1,4,7-tri-azacyclononane) with substituted benzoic acid or phenylacetic acid, in water in the presence of potassium hexafluorophosphate gave a series of cationic dinuclear Ru(III)-Ru(III) (mu-oxo)bis(mu-carboxylato) complexes [(Me3tacn)2Ru2(mu-O)(mu-OOCR)2](PF6)2 (R = Ph, 1; -py, 2; -C6H4-2-Cl, 3; -C6H3-2,4-Cl2, 4; -CH2C6H4-2-CH3, 5; -CH2C6H4-4-CH3, 6; -CH2C6H4-4-OCH3, 7; -CH2C6H4-4-Cl, 8). All complexes are well characterized by infrared, UV/Vis and mass spectroscopies, and their electrochemical properties were also investigated. The molecular structures of 1, 2 center dot 2C3H6O, 5 center dot 2C3H6O, 7 and 8 have been also established by single-crystal X-ray diffraction. The photocatalytic properties for H2 evolution by water splitting of complexes 1, 2, 3, 5, and 7 were also investigated in the paper.

Welcome to talk about 50-84-0, If you have any questions, you can contact Qian, BF; Wang, JL; Jia, AQ; Shi, HT; Zhang, QF or send Email.. Recommanded Product: 50-84-0

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Recently I am researching about KINETIC DIASTEREOSELECTIVE ACYLATION; ALKYLATING-AGENTS; GLYCOSYL DONORS; IN-VITRO; GLUCURONIDES; DERIVATIVES; OXIDATION; GLUCOSIDES; DELIVERY; ESTERS, Saw an article supported by the CNRSCentre National de la Recherche Scientifique (CNRS)European Commission; University Paris-Sud; ANRFrench National Research Agency (ANR) [ANR-15-CE29-0002]; Ligue Contre le Cancer through an Equipe Labellisee 2014 grant; Algerian Ministry of Education and Research; [ANR-10-LABX-33]. SDS of cas: 50-84-0. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Bennai, N; Chabrier, A; Fatthalla, MI; Tran, C; Yen-Pon, E; Belkadi, M; Alami, M; Grimaud, L; Messaoudi, S. The CAS is 50-84-0. Through research, I have a further understanding and discovery of 2,4-Dichlorobenzoic acid

We have discovered a new mode of reactivity of 1-thiosugars in the presence of Cu(II) or Co(II) for a stereoselective O-glycosylation reaction. The process involves the use of a catalytic amount of Cu(acac)(2) or Co(acac)(2) and Ag2CO3 as an oxidant in alpha,alpha,alpha-trifluorotoluene. Moreover, this protocol turned out to have a broad scope, allowing the preparation of a wide range of complex substituted O-glycoside esters in good to excellent yields with an exclusive 1,2-trans-selectivity. The late-stage modification of pharmaceuticals by this method was also demonstrated. To obtain a closer insight into the reaction mechanism, cyclic voltammetry was performed.

About 2,4-Dichlorobenzoic acid, If you have any questions, you can contact Bennai, N; Chabrier, A; Fatthalla, MI; Tran, C; Yen-Pon, E; Belkadi, M; Alami, M; Grimaud, L; Messaoudi, S or concate me.. SDS of cas: 50-84-0

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Formula: C7H4Cl2O2. In 2021 CHEMMEDCHEM published article about CANDIDA-ALBICANS; FUNGAL-INFECTIONS; CYP51; ASPERGILLOSIS; MECHANISMS; DIAGNOSIS; AGENTS in [Zoidis, Grigoris] Natl & Kapodistrian Univ Athens, Dept Pharm, Athens 15771, Greece; [Kritsi, Eftichia; Zoumpoulakis, Panagiotis] Natl Hellen Res Fdn, Inst Chem Biol, Vas Constantinou Ave 48, Athens 11635, Greece; [Lecinska, Paulina; Catto, Marco] Univ Bari Aldo Moro, Dipartimento Farm Sci Farmaco, Via E Orabona 4, I-70125 Bari, Italy; [Ivanov, Marija; Sokovic, Marina] Univ Belgrade, Natl Inst Republ Serbia, Inst Biol Res Sinisa Stankovic, Bulevar Despota Stefana 142, Belgrade 11000, Serbia in 2021, Cited 39. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0.

The significant antifungal activity of a series of novel 1,2,4-triazole derivatives against different strains ofCandida albicans,Candida kruseiandAspergillus fumigatus, compared to the commercial fungicides ketoconazole and itraconazole, is reported. Systemic mycosis and invasive fungal infections, whether from immunodeficiency or hospital-acquired infection, have been on an upward trend for several years. The 1,2,4-triazole ring substituted with other aromatic and heteroaromatic systems plays an important role in the field of antifungal drug discovery and development. Thus, an extensive series of 29 triazoles, substituted in different positions with a variety of aromatic rings, has been designed, synthesized, and evaluated for their fungicidal activity. Almost all the agents testedin vitroshowed high activity against all examined fungal strains. It is noteworthy that, in the case ofA. fumigatus, all the examined compounds achieved equal or higher antifungal activity than ketoconazole, but less activity than itraconazole. Among all the derivatives studied, the dichlorourea analogue and bromo-substituted triazole stand out as the most promising compounds. Quantitative structure-activity relationship (QSAR) models were built for a systematic structure-activity relationship (SAR) profile to explain and potentially explore the potency characteristics of 1,2,4-triazole analogues.

Bye, fridends, I hope you can learn more about C7H4Cl2O2, If you have any questions, you can browse other blog as well. See you lster.. Formula: C7H4Cl2O2

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Liu, WJ; Xu, JM; Chen, XH; Zhang, FX; Xu, ZF; Wang, DP; He, YQ; Xia, XH; Zhang, X; Liang, Y in [Liu, Wenjie; Xu, Jiamin; Chen, Xiahong; Zhang, Fuxing; Xu, Zhifeng; Wang, Deping; Zhang, Xin] Hengyang Normal Univ, Coll Chem & Mat Sci, Key Lab Funct Organometall Mat, Hengyang 421008, Hunan, Peoples R China; [He, Yongqiang; Xia, Xiaohong] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Hunan, Peoples R China; [Zhang, Xin; Liang, Yun] Hunan Normal Univ, Coll Chem & Chem Engn, Changsha 410081, Peoples R China published CuI/2-Aminopyridine 1-Oxide Catalyzed Amination of Aryl Chlorides with Aliphatic Amines in 2020.0, Cited 121.0. HPLC of Formula: C7H7Cl. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

A class of 2-aminopyridine 1-oxides are discovered to be effective ligands for the Cu-catalyzed amination of less reactive (hetero)aryl chlorides. A wide range of functionalized (hetero)aryl chlorides reacted with various aliphatic amines to afford the desired products in good to excellent yields under the catalyst of CuI/2-aminopyridine 1-oxides. Furthermore, the catalyst system worked well for the coupling of cyclic secondary amines and N-methyl benzylamine with (hetero)aryl chlorides.

HPLC of Formula: C7H7Cl. Bye, fridends, I hope you can learn more about C7H7Cl, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

In 2021.0 CHEMISTRYSELECT published article about NUCLEOPHILIC BEHAVIOR; DBU; REARRANGEMENT; PALLADIUM; NITROGEN; AMIDES; AMINE; WATER in [Babu, Gogu V. Surendra; Bhaskaran, Aathira; Sridhar, Balasubramanian; Rao, Tumula Venkateshwar; Parvathaneni, Sai Prathima] CSIR Indian Inst Chem Technol, Catalysis & Fine Chem Div, Hyderabad 500607, Telangana, India; [Babu, Gogu V. Surendra] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India in 2021.0, Cited 42.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Formula: C7H7Cl

This paper demonstrates a selective, mild approach to Ullmann amination of aryl halides to synthesize N-alkylated derivatives of epsilon-caprolactam. The synthetic route involves an in-situ ring-opening of 1,8-diazabicyclo[5.4.0]undec-8-ene (DBU) followed by concurrent arylation with aryl halides in the presence of copper iodide as a catalyst under ligand-free conditions. This method provides a new entry to a wide variety of epsilon-caprolactam derivatives in good to excellent yields in a single synthetic sequence. Similarly, other bicyclic amidines such as 1, 5-diazabicyclo-[4.3.0]non-5-ene (DBN), and 1,5,7 triazabicyclo[4.4.0] dec-5-ene (TBD) also showed good to very high reactivity. Azepan-2-one, or Caprolactam, is an important synthon in polymer chemistry and has a global demand as it is employed to make Nylon 6 filament, fiber, and plastics.([1]) The global caprolactam market size is expected to expand for the growing textile industry with rising demand for plastics in the construction of automotive, electrical, and electronic sectors. Additionally, technological advancements aimed at improving the cost-effective manufacturing process of caprolactam, to minimize the release of hazardous waste into the environment is of vital necessity. Derivatives of epsilon-caprolactam are of interest for the production of modified nylons([2]) and nanogels.([3]) Several Azepinones and their analogs play an important role in medicinal chemistry,([4]) used in the synthesis of pharmaceutical drugs including Benazepril,([5]) Telcagepant,([6]) and Ivabradine.([7])

Formula: C7H7Cl. Welcome to talk about 95-49-8, If you have any questions, you can contact Babu, GVS; Bhaskaran, A; Sridhar, B; Rao, TV; Parvathaneni, SP or send Email.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics