Month: October 2022

The author of 《An Efficient Sequential One-Pot Approach for the Synthesis of C3-Functionalized Imidazo[1,2-a]pyridines under Transition-Metal Free Conditions》 were Reddy, Raju Jannapu; Shankar, Angothu; Kumari, Arram Haritha. And the article was published in Asian Journal of Organic Chemistry in 2019. Application of 882-33-7 The author mentioned the following in the article:

A metal-free sequential one-pot three-component protocol is described for the synthesis of C3-functionalized imidazo[1,2-a]pyridines. A successive construction of imidazo[1,2-a]pyridine I (R = 4-MeC6H4, 2-naphthyl, 2-thienyl, etc.; R1 = SMe, naphthalen-1-ylsulfanyl, pyridin-2-ylsulfanyl, etc.; X = H, 6-Br, 6-Cl, 7-Me, 8-Me) followed by iodine-catalyzed sulfenylation has been achieved in a one-pot operation from readily available α-bromomethyl ketones RC(O)CH2Br, 2-aminopyridines II and thiosulfonates R1S(O)2Ar (Ar = C6H5, 1-naphthyl, 2-thienyl, etc.). An immense array of 3-sulfenylimidazo[1,2-a]pyridines I was obtained in good to high yields. Also, the method is extended for the synthesis of C3-halogenated imidazo[1,2-a]pyridines I (R1 = Br, Cl) using sodium halides NaY in the presence of K2S2O8. Notably, the reaction between α-bromomethyl ketones and 2-aminopyridines in the presence of K2S2O8 to yields 3-bromo-2-aryl-imidazo[1,2-a]pyridines I (R1 = Br), thus implying α-bromomethyl ketones to be served as brominating agent. Overall, the present sequential one-pot protocol is straightforward, operationally simple, tolerates a broad range of functional groups, and is reliable for gram-scale experiments In the experimental materials used by the author, we found 1,2-Diphenyldisulfane(cas: 882-33-7Application of 882-33-7)

1,2-Diphenyldisulfane(cas: 882-33-7) belongs to ethers.Although ethers resist hydrolysis, they are cleaved by hydrobromic acid and hydroiodic acid. Hydrogen chloride cleaves ethers only slowly. Application of 882-33-7

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Synthesis and evaluation of antimicrobial and antioxidant activity of novel 7-Aryl-6H,7H-benzo[f]chromeno[4,3-b]chromen-6-one by MgO nanoparticle as green catalyst》 was published in Journal of Heterocyclic Chemistry in 2020. These research results belong to Hosseinzadegan, Sara; Hazeri, Nourallah; Maghsoodlou, Malek T.. Formula: C8H8O3 The article mentions the following:

Novel 7-aryl-6H,7H-benzo[f]chromeno[4,3-b]chromen-6-one derivatives I [R = C6H5, 4-MeOC6H4, 3-O2NC6H4, etc.] were synthesized via multicomponent reaction of 2-naphthol, aldehyde derivatives, 4-hydroxycoumarin using MgO nanoparticles as a recyclable and efficient catalyst. This method offered some benefits such as shorter time, high yields and concordance with green chem. All the synthesized compounds were evaluated for their antibacterial, antifungal and antioxidant activities. The results came from multiple reactions, including the reaction of 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Formula: C8H8O3)

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Formula: C8H8O3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Introduction of a new bis-derivative of succinimide (Bis-Su) as a sustainable and efficient basic organo-catalyst for the synthesis of arylidene malononitrile and tetrahydrobenzo[b]pyran derivatives under green conditions》 was published in Research on Chemical Intermediates in 2020. These research results belong to Hassanzadeh, Fariba; Daneshvar, Nader; Shirini, Farhad; Mamaghani, Manouchehr. Product Details of 135-02-4 The article mentions the following:

In this work, a new bis-succinimide (Bis-Su) compound 1-[4-(2,5-dioxopyrrolidin-1-yl)butyl]pyrrolidine-2,5-dione is prepared, identified and used as a green and efficient basic organo-catalyst for the promotion of the synthesis of arylidene malononitriles ArCH=C(CN)2 (Ar = C6H5, 4-ClC6H4, (E)-4-NO2C6H4CH=CH, etc.) and tetrahydrobenzo[b]pyrans I. Using this method, both of the reactions were performed under mild conditions, during short reaction times in high yields. The catalyst can also be recycled and reused several times without a considerable decrease in its activity. In the experiment, the researchers used 2-Methoxybenzaldehyde(cas: 135-02-4Product Details of 135-02-4)

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.Product Details of 135-02-4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Ultrasound assisted eco-friendly synthesis of 3-cinnamoyl coumarins using N,N’-(1,2-phenylene)bis(2-aminobenzamide)dichloro cobalt immobilized on mesoporous Al-SBA-15 as a new and recyclable catalyst》 was published in Green Chemistry Letters and Reviews in 2020. These research results belong to Akbarzadeh, Zeinab; Safaei-Ghomi, Javad. Safety of 2-Hydroxy-4-methoxybenzaldehyde The article mentions the following:

A novel mesoporous Al-SBA-15 modified by N,N’-(1,2-phenylene)bis(2-aminobenzamide) dichloro cobalt has been prepared and applied as a reusable catalyst in the 3-cinnamoyl coumarins I (R = 4-Br, 2-OH, 4-F, etc.; R1 = H, 7-OMe, 6-OMe, 6-Br) synthesis via three-component reaction between benzaldehydes RC6H4CHO, salicylaldehydes like salicylaldehyde, 2-hydroxy-4-methoxybenzaldehyde, 2-hydroxy-5-methoxybenzaldehyde, 5-bromo-2-hydroxybenzaldehyde and Et acetoacetate by the assist of ultrasonic irradiation By using the nanocatalyst and also ultrasound irradiation, the facility and velocity of the above mentioned reaction were enhanced and an environment friendly condition was provided to synthesis of various 3-cinnamoyl coumarin compounds I. The properties and structure of nanocatalyst have been specified by methods including powder X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), Fourier transform IR spectroscopy (FT-IR), transmission electron microscopy (TEM), nitrogen adsorption-desorption anal. and scanning electronic microscopy (SEM). Superiority of this novel and viable method is due to mild reaction condition, short reaction times, high yields of 3-cinnamoyl coumarins I, environmentally benign, recoverability of the CoCl2N,N’-(1,2-phenylene)bis (2-aminobenzamide)/Al-SBA-15 catalyst and reusability with important preservation in its catalytic activity. The experimental process involved the reaction of 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Safety of 2-Hydroxy-4-methoxybenzaldehyde)

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Safety of 2-Hydroxy-4-methoxybenzaldehyde

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Empirical Models of Stability of Crown Ether Complexes with Alkaline and Alkaline-Earth Metals in Selected Pure Solvents》 was published in Russian Journal of General Chemistry in 2020. These research results belong to Bondarev, N. V.. Product Details of 33100-27-5 The article mentions the following:

An approach to predict the stability constants of coronates from the properties of solvents, cations, and crown ethers has been developed based on exploratory and neural network methods for math. modeling of equilibrium in solutions Exploratory (factor, cluster, discriminant, canonical, decision trees), regression, and neural network (supervised and Kohonen network) models of the stability of crown ethers (12C4, 13C4, 14C4, 15C4, 15C5, 18C6, 21C7, 24C8, B12C4, B15C5, CH15C5, CH18C6, DCH18C6, DCH21C7, DB18C6, DB21C7, DB24C8, DB27C9, and DB30C10) complexes with cations of alkali (Li+, Na+, K+, Cs+, Rb+) and alk.-earth (Ca2+, Sr2+, Ba2+) metals in aqueous and non-aqueous (acetone, acetonitrile, DMSO, methanol, pyridine, DMF, dioxane, propylene carbonate, 1,2-dichloroethane, and nitrobenzene) solutions have been developed according to the properties of solvents (diameter of solvent mol., Kamlet-Taft parameter, Dimroth-Reichardt parameter, dielec. constant), crown ethers (Balaban topol. index), and cations (cation diameter) at 298.15 K.1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5Product Details of 33100-27-5) was used in this study.

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Product Details of 33100-27-5

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Synthesis and Anti-Microbial Activity of Benzylidenhydrazides of Glycyrrhetic Acid》 was written by Baltina, L. A.; Kondratenko, R. M.; Bulgakov, A. K.. COA of Formula: C8H8O2 And the article was included in Russian Journal of Bioorganic Chemistry in 2020. The article conveys some information:

New derivatives of glycyrrhetic acid with hydrazide pharmacophore groups I (R = C6H5, 4-HOC6H4, 4-MeOC6H4, 2-MeOC6H4, 4-(Me)2NC6H3) were synthesized and their antimicrobial activity was evaluated. Compound I (R = 4-HOC6H4) exhibited the highest antimicrobial activity. This compound had both an antibacterial effect against Escherichia coli, Proteus vulgaris, Klebsiella pneumonia, Staphylococcus aureus, Citrobacter diversus, Enterobacter aerogenes, Pseudomonas aeruginosa, and Enterobacter cloacae and antifungal activity against the Candida albicans fungus. The min. inhibitory concentrations of this compound and pimafucin were similar for Candida albicans. In the part of experimental materials, we found many familiar compounds, such as 2-Methoxybenzaldehyde(cas: 135-02-4COA of Formula: C8H8O2)

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.COA of Formula: C8H8O2

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Devulcanization of natural rubber industry waste in supercritical carbon dioxide combined with diphenyl disulfide》 was written by Asaro, Lucia; Gratton, Michel; Poirot, Nathalie; Seghar, Said; Ait Hocine, Nourredine. COA of Formula: C12H10S2 And the article was included in Waste Management (Oxford, United Kingdom) in 2020. The article conveys some information:

The elimination of rubber wastes without affecting the environment is one of the most important challenges of the 21st century waste management. Accordingly, the present work is focused on the recycling of natural rubber (NR) industry waste by means of devulcanization in supercritical carbon dioxide (scCO2) atm. With that aim, a novel device allowing to perform rubber devulcanization was developed. It consists of a triaxial compression reactor integrated into a dynamic hydraulic universal testing machine with a heating chamber. NR industry waste was devulcanized in the mentioned device at different temperatures, in scCO2 by using di-Ph disulfide (DD) as devulcanizing reagent. The devulcanization degree and quality of the treated materials were evaluated by the swelling test combined with the Horikx theory. It was appeared that a successful devulcanization, with almost no degradation, was obtained, and the devulcanization degree reached maximum value of ∼90%. Thermogravimetric tests and SEM (SEM) images strengthened these results. Finally, it was concluded that the developed device is appropriate to perform rubber recycling, which contributes to the progress in the environmental protection. In the experimental materials used by the author, we found 1,2-Diphenyldisulfane(cas: 882-33-7COA of Formula: C12H10S2)

1,2-Diphenyldisulfane(cas: 882-33-7) belongs to ethers.Ethers do have nonbonding electron pairs on their oxygen atoms, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. COA of Formula: C12H10S2 The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

《Acne and rosacea in skin of colour.》 was written by Maruthappu, T; Taylor, M. Recommanded Product: 106685-40-9 And the article was included in Clinical and experimental dermatology in 2021. The article conveys some information:

Acne and rosacea are common inflammatory skin conditions present in numerous racial and ethnic groups. There are distinct differences in clinical presentation, exacerbating factors, potential triggers and consequences of both conditions in individuals with skin of colour (SOC), classified as Fitzpatrick skin types III-VI. For example, acne can be complicated by the development of postinflammatory hyperpigmentation and keloid scarring in SOC, and this can influence treatment choice. Although rosacea is reported less frequently in SOC, this may be the result of delayed diagnosis or late presentation due to the difficulty in discerning the classic features of erythema in darker skin tones. In such cases, additional clues in the medical history and clinical examination may assist in making the diagnosis. This review aims to summarize nuances in both the diagnosis and management of these two common skin conditions in patients with SOC to support clinicians in providing an individualized treatment approach. In the experiment, the researchers used many compounds, for example, 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid(cas: 106685-40-9Recommanded Product: 106685-40-9)

6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid(cas:106685-40-9) may be used as a pharmaceutical reference standard for the quantification of the analyte in topical gel formulations using high-performance liquid chromatography technique.Recommanded Product: 106685-40-9

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Li, Zezhong John; Srebnik, Simcha published their research in Physical Chemistry Chemical Physics in 2021. The article was titled 《Expanding carbon capture capacity: uncovering additional CO2 adsorption sites in imine-linked porous organic cages》.Related Products of 33100-27-5 The article contains the following contents:

With an increasing need to develop carbon capture technologies, research regarding the use of cage-based porous materials has garnered great interest. Typically, the study of gas adsorption in porous organic cages (POCs) has focused on the gas uptake inside the cage cavity. By using mol. dynamics simulation, this study reveals the presence of eight sites outside the cavity of a 15-crown-5 ether-substituted imine-linked POC which could enhance carbon dioxide adsorption capacity. Adsorption on these sites is likely stabilized by the functional groups on the cage vertices and the imine groups on the faces of the POC. These external adsorption sites have a higher CO2 adsorption capacity and greater sensitivity to temperature and pressure changes than the sites within the cage cavity. These characteristics are particularly favorable for applications based on pressure- and temperature-swing separation In the experimental materials used by the author, we found 1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5Related Products of 33100-27-5)

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Related Products of 33100-27-5

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Gamez, Francisco; Aviles-Moreno, Juan R.; Berden, Giel; Oomens, Jos; Martinez-Haya, Bruno published their research in Physical Chemistry Chemical Physics in 2021. The article was titled 《Proton in the ring: spectroscopy and dynamics of proton bonding in macrocycle cavities》.Reference of 1,4,7,10,13-Pentaoxacyclopentadecane The article contains the following contents:

The proton bond is a paradigmatic quantum mol. interaction and a major driving force of supramol. chem. The ring cavities of crown ethers provide an intriguing environment, promoting competitive proton sharing with multiple coordination anchors. This study shows that protons confined in crown ether cavities form dynamic bonds that migrate to varying pairs of coordinating atoms when allowed by the flexibility of the macrocycle backbone. Prototypic native crown ethers (12-crown-4, 15-crown-5 and 18-crown-6) and aza-crown ethers (cyclen, 1-aza-18-crown-6 and hexacyclen) are investigated. For each system, IR action spectroscopy experiments and ab initio Mol. Dynamics computations are employed to elucidate the structural effects associated with proton diffusion and its entanglement with the conformational and vibrational dynamics of the protonated host. The experimental part of the paper was very detailed, including the reaction process of 1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5Reference of 1,4,7,10,13-Pentaoxacyclopentadecane)

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Reference of 1,4,7,10,13-Pentaoxacyclopentadecane

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem