Fan, Xiaodong’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2022 | CAS: 2398-37-0

1-Bromo-3-methoxybenzene(cas: 2398-37-0) can be used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemicals.COA of Formula: C7H7BrO

COA of Formula: C7H7BrOIn 2022 ,《Visible light-induced deoxygenation/cyclization of salicylic acid derivatives and aryl acetylene for the synthesis of flavonoids》 was published in Chemical Communications (Cambridge, United Kingdom). The article was written by Fan, Xiaodong; He, Chaoyin; Ji, Mengmeng; Sun, Xinhui; Luo, Huan; Li, Chao; Tong, Huixin; Zhang, Weiya; Sun, Zhizhong; Chu, Wenyi. The article contains the following contents:

A visible-light-induced photocatalytic strategy for the synthesis of flavonoids was developed through the deoxygenative/cyclization reaction of salicylic acid derivatives with aryl acetylene using di-Ph sulfide as an O-transfer reagent. Based on the controlled experiments, the mechanism of visible-light-induced free radical coupling cyclization was proposed. The protocol obtained 51 flavonoids in good yields and was successfully applied to the synthesis of some natural flavones. In the part of experimental materials, we found many familiar compounds, such as 1-Bromo-3-methoxybenzene(cas: 2398-37-0COA of Formula: C7H7BrO)

1-Bromo-3-methoxybenzene(cas: 2398-37-0) can be used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemicals.COA of Formula: C7H7BrO

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

Jin, Guo Jun’s team published research in Transition Metal Chemistry (Dordrecht, Netherlands) in 2011 | CAS: 74029-40-6

1,4-Diethynyl-2,5-dimethoxybenzene(cas: 74029-40-6) belongs to ethers.Category: ethers-buliding-blocksAlthough ethers resist hydrolysis, they are cleaved by hydrobromic acid and hydroiodic acid. Hydrogen chloride cleaves ethers only slowly.

Category: ethers-buliding-blocksOn September 30, 2011 ,《Synthesis, characterization, and properties of conjugated binuclear bis-terpyridyl ruthenium complexes》 was published in Transition Metal Chemistry (Dordrecht, Netherlands). The article was written by Jin, Guo Jun; Chen, Gang; Xia, Jian Long; Yin, Jun; Yu, Guang-Ao; Liu, Sheng Hua. The article contains the following contents:

A series of binuclear bis-terpyridyl ruthenium complexes with different substituents, [Ru2(L)2(μ-La)](PF6)4 (L = 4′-(p-tolyl)-4,4”-dicarboxyterpyridine, La = 1,4-bis(4-(4,4”-dicarboxyterpyrid-4′-yl)phenylethynyl)-2,5-R2-benzene, R = H, Me, OMe, OC6H13) were synthesized and characterized by physicochem. and spectroscopic methods. The UV/visible and fluorescence spectra indicated that the non-substituted binuclear bis(terpyridyl) ruthenium(II) complex has similar properties to those with electron-donating groups such as Me and alkoxyl on the organic conjugated bridge benzene units. Furthermore, similar oxidation-reduction potentials were observed according to their electrochem. properties in CH2Cl2 solution In addition to this study using 1,4-Diethynyl-2,5-dimethoxybenzene, there are many other studies that have used 1,4-Diethynyl-2,5-dimethoxybenzene(cas: 74029-40-6Category: ethers-buliding-blocks) was used in this study.

1,4-Diethynyl-2,5-dimethoxybenzene(cas: 74029-40-6) belongs to ethers.Category: ethers-buliding-blocksAlthough ethers resist hydrolysis, they are cleaved by hydrobromic acid and hydroiodic acid. Hydrogen chloride cleaves ethers only slowly.

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

Guanziroli, Elena’s team published research in Italian journal of dermatology and venereology in 2018 | CAS: 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.Application of 106685-40-9

In 2018,Guanziroli, Elena; Venegoni, Luigia; Fanoni, Daniele; Cavicchini, Stefano; Coggi, Antonella; Ferrero, Stefano; Gianotti, Raffaele; Berti, Emilio; Del Gobbo, Alessandro published 《Immunohistochemical expression and prognostic role of CD10, CD271 and Nestin in primary and recurrent cutaneous melanoma.》.Italian journal of dermatology and venereology published the findings.Application of 106685-40-9 The information in the text is summarized as follows:

BACKGROUND: CD10, CD271 and Nestin, which are proteins associated with tumor-initiating properties and/or progression potential, have not been specifically studied on malignant melanoma (MM) with cutaneous recurrences. METHODS: We evaluated the expression of CD10, CD271 and Nestin in 27 tumor samples from 16 patients. These tumor samples corresponded to 6 primary melanomas which developed 11 ITM and 10 primary melanomas without recurrences at 10-year follow-up from specimens obtained from surgical excisions of patients referred to the Unit of Dermatology, Department of Medical-Surgical and Transplant Physiopathology, University of Milan, between 2006 and 2016. RESULTS: We demonstrated a higher expression of CD271 and Nestin in primary tumors which recurred than control population, Nestin was expressed with significantly higher percentages in primary tumors than recurrences, and CD10 expression was statistically significant correlated with disease-free survival: cases with a lower score recurred lately than cases with higher scores. CONCLUSIONS: Our preliminary results suggested that CD271 and Nestin can be considered early biomarkers for the development of ITM, Nesting can be useful in differentiating primary MM from cutaneous recurrences and CD10 is associated with a rapid disease progression and may be considered a potential prognostic marker. In the part of experimental materials, we found many familiar compounds, such as 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid(cas: 106685-40-9Application of 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.Application of 106685-40-9

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

Medina, David X.’s team published research in Journal of Drug Delivery Science and Technology in 2019 | CAS: 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.Application In Synthesis of 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid

In 2019,Journal of Drug Delivery Science and Technology included an article by Medina, David X.; Chung, Eugene P.; Bowser, Robert; Sirianni, Rachael W.. Application In Synthesis of 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid. The article was titled 《Lipid and polymer blended polyester nanoparticles loaded with adapalene for activation of retinoid signaling in the CNS following intravenous administration》. The information in the text is summarized as follows:

Small mol. retinoids are potential therapeutics for a variety of neurol. diseases. However, most retinoids are poorly water soluble and difficult to deliver in vivo, which prevents further study of their utility to treat disease. Here, we focus on adapalene, an FDA approved drug that is a specific agonist for the retinoic acid receptor β (RARβ). We sought to develop nanoparticle delivery systems that would enable effective delivery of adapalene to the CNS. We developed strategies to produce nanoparticles based on the hypothesis that incorporation of hydrophobic mols. into a polyester base would improve adapalene loading. In the first scheme, poly(lactic acid)-poly(ethylene glycol) (PLA-PEG) was blended with low mol. weight poly(lactic acid) (PLA) or poly(caprolactone) (PCL). In the second scheme, poly(lactic-co-glycolic acid) (PLGA) was blended with 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino (polyethylene glycol)] (DSPE-PEG). Our data demonstrate that blending low mol. weight polyesters or DSPE-PEG into the primary nanoparticle base improves encapsulation of adapalene, presumably by enhancing adapalene solubility in the nanoparticle. Peripheral administration of these nanoparticles activated retinoid signaling in the brain and spinal cord of healthy mice. These studies provide new approaches for nanoparticle fabrication and establish proof of principle that systemically administered, adapalene-loaded nanoparticles activate retinoid signaling in the CNS. In the experiment, the researchers used many compounds, for example, 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid(cas: 106685-40-9Application In Synthesis of 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid)

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.Application In Synthesis of 6-(3-(Adamantan-1-yl)-4-methoxyphenyl)-2-naphthoic acid

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

An, Na’s team published research in Methods in Molecular Biology (New York, NY, United States) in 2019 | CAS: 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. SDS of cas: 33100-27-5

The author of 《Synthesis of site-specific crown ether adducts to DNA abasic sites: 8-oxo-7,8-dihydro-2′-deoxyguanosine and 2′-deoxycytidine》 were An, Na; Fleming, Aaron M.; Rosecrans, Nicole C.; Liao, Yi; Burrows, Cynthia J.. And the article was published in Methods in Molecular Biology (New York, NY, United States) in 2019. SDS of cas: 33100-27-5 The author mentioned the following in the article:

Formation of adducts to DNA is of great benefit to DNA sequencing and damage detection technol. and to enzymol. Here we describe the synthesis and characterization procedures of 18-crown-6 adducts formed to abasic (AP) sites, 8-oxo-7,8-dihydro-2′-deoxyguanosine (OG), and 2′-deoxycytidine (C) residues in DNA oligodeoxynucleotides. These crown ether adducts were used as site-specific modifications to facilitate nanopore technol. The methods described can be readily expanded to attach other suitable primary amines of interest. The results came from multiple reactions, including the reaction of 1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5SDS of cas: 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. SDS of cas: 33100-27-5

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

Wang, Wenqing’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2020 | CAS: 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. Synthetic Route of C10H20O5

《Stable, yet “”naked””, azo radical anion ArNNAr- and dianion ArNNAr2- (Ar = 4-CN-2,6-iPr2-C6H2) with selective CO2 activation》 was published in Chemical Communications (Cambridge, United Kingdom) in 2020. These research results belong to Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping. Synthetic Route of C10H20O5 The article mentions the following:

Azo radical anion (1-̇) and dianion 12- were isolated by 1- and two-electron reduction of the azo compound 1 (ArNNAr, Ar = 4-CN-2,6-iPr2-C6H2) with alkali metals, resp. The reduced species were characterized by single-crystal x-ray anal., EPR, UV and FTIR spectroscopy, as well as SQUID measurements. The filling of one and two electrons in the π* orbital of the N-N double bond of 1 leads to a half-double N-N bond in 1-̇ and a single N-N bond in 12-. The uncoordinated nature of these reduced species enables them to activate CO2. The exposure of 1 ̇- solution to CO2 gave oxalate anion C2O42-, while that of 12- solution to CO2 afforded the hydrazine dicarboxylate dianion [1-2CO2]2-, which is reversibly dissociated back to 1 and CO2 upon oxidation In the experiment, the researchers used many compounds, for example, 1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5Synthetic Route of C10H20O5)

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. Synthetic Route of C10H20O5

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

Rodrigues, Vereena’s team published research in In Vitro Cellular & Developmental Biology: Plant in 2020 | CAS: 673-22-3

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.SDS of cas: 673-22-3

《Micropropagation, encapsulation, and conservation of Decalepis salicifolia, a vanillin isomer containing medicinal and aromatic plant》 was published in In Vitro Cellular & Developmental Biology: Plant in 2020. These research results belong to Rodrigues, Vereena; Kumar, Amit; Gokul, Sivaraman; Verma, Ram S.; Rahman, Laiq ur; Sundaresan, Velusamy. SDS of cas: 673-22-3 The article mentions the following:

Abstract: An efficient in vitro propagation and synthetic seed production protocol was established for the conservation of Decalepis salicifolia (Bedd. ex Hook.f.) Venter, an endemic and critically endangered ethnomedicinal species. Axillary bud proliferation was found to be best in 11.1μM BAP with an average of 3.5 ± 0.06 shoots per explant. Shoot tip and nodal explants were encapsulated in sodium alginate and their regeneration was achieved following storage at 4°C up to 12 wk. Successful rooting was obtained in modified MS medium with low nitrate and high sucrose concentration Quarter strength MS media containing 2.5 mM each of NH4NO3 and KNO3 along with 8% sucrose produced an average number of 12.4 ± 1.18 roots with an average length of 4.3 ± 0.08 cm. The in vitro derived rooted plants were successfully hardened (92.8%) and established in field with 100.0% survival rate. Inter-simple sequence repeat (ISSR) markers proved the genetic fidelity among the in vitro grown plant showing 99.5% similarity with the mother plant. Micropropagation derived acclimatized plants produced 2-hydroxy-4-methoxybenzaldehyde in amounts similar to seed-derived field-grown plants of the same age. The in vitro propagation protocol developed for D. salicifolia can be utilized to reduce exploitation pressure from their natural habitats and augment ecorestoration, conservation, and cultivation of this critically endangered and industrially valuable plant. In the experiment, the researchers used many compounds, for example, 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3SDS of cas: 673-22-3)

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.SDS of cas: 673-22-3

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

Zhang, Bo-Sheng’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2020 | CAS: 529-28-2

1-Iodo-2-methoxybenzene(cas: 529-28-2) participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations.Quality Control of 1-Iodo-2-methoxybenzene

《DMAP and PivOH-promoted amination/allenization reaction》 was published in Chemical Communications (Cambridge, United Kingdom) in 2020. These research results belong to Zhang, Bo-Sheng; Li, Yuke; Gou, Xue-Ya; Zhang, Zhe; An, Yang; Wang, Xin-Gang; Liang, Yong-Min. Quality Control of 1-Iodo-2-methoxybenzene The article mentions the following:

This report described the first DMAP and PivOH-promoted ortho-C-H amination and ipso-allenization reaction of iodobenzenes realized by Pd/norbornene cooperative catalysis. Based on control experiments and DFT calculations, the authors speculated that the three ligands have different functions and mechanism paths in the reaction. In the experiment, the researchers used many compounds, for example, 1-Iodo-2-methoxybenzene(cas: 529-28-2Quality Control of 1-Iodo-2-methoxybenzene)

1-Iodo-2-methoxybenzene(cas: 529-28-2) participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations.Quality Control of 1-Iodo-2-methoxybenzene

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

Kundu, Samrat’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2021 | CAS: 60656-87-3

2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) may be used in the following syntheses: (3S,5S)-methyl 6-benzyloxy-3,5-dihydroxyhexanoate ,(S)-5-benzyloxy-4-hydroxypentan-2-one, myxothiazols.Recommanded Product: 2-(Benzyloxy)acetaldehyde

Kundu, Samrat; Banerjee, Ankush; Pal, Shyam Chand; Ghosh, Meghna; Maji, Modhu Sudan published their research in Chemical Communications (Cambridge, United Kingdom) in 2021. The article was titled 《Cascade annulative π-extension for the rapid construction of carbazole based polyaromatic hydrocarbons》.Recommanded Product: 2-(Benzyloxy)acetaldehyde The article contains the following contents:

A Bronsted acid catalyzed cascade benzannulation strategy for the one-pot synthesis of densely populated poly-aryl benzo[a]carbazole architectures is disclosed from easily affordable fundamental commodities. The efficacy of this technique was further validated via the concise synthesis of structurally unique carbazole based poly-aromatic hydrocarbons. Furthermore, the photo-phys. properties of the synthesized compounds are thoroughly investigated. The experimental part of the paper was very detailed, including the reaction process of 2-(Benzyloxy)acetaldehyde(cas: 60656-87-3Recommanded Product: 2-(Benzyloxy)acetaldehyde)

2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) may be used in the following syntheses: (3S,5S)-methyl 6-benzyloxy-3,5-dihydroxyhexanoate ,(S)-5-benzyloxy-4-hydroxypentan-2-one, myxothiazols.Recommanded Product: 2-(Benzyloxy)acetaldehyde

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

Cano, Carolina’s team published research in European Journal of Medicinal Chemistry in 2009-12-31 | 10305-42-7

European Journal of Medicinal Chemistry published new progress about Cannabinoid receptor 1 Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 10305-42-7 belongs to class ethers-buliding-blocks, and the molecular formula is C3H8ClNO2S, Recommanded Product: n-Propylsulphamoyl chloride.

Cano, Carolina; Paez, Juan Antonio; Goya, Pilar; Serrano, Antonia; Pavon, Javier; Rodriguez de Fonseca, Fernando; Suardiaz, Margarita; Martin, Maria Isabel published the artcile< Synthesis and pharmacological evaluation of sulfamide-based analogues of anandamide>, Recommanded Product: n-Propylsulphamoyl chloride, the main research area is anandamide sulfamide derivative preparation CB1 receptor affinity structure activity.

Arachidonyl and linoleyl sulfamide derivatives have been synthesized and their potential cannabimimetic properties evaluated in in vitro functional and binding assays. Replacement of the ethanolamide moiety of anandamide by -CH2NHSO2NH-R (R = saturated or unsaturated long chain alkyl, adamantyl derivative) considerably reduces the CB1 receptor activity and only some of the compounds showed modest cannabinoid properties in binding assays. The new compounds were also tested as inhibitors of the FAAH enzyme but were inactive.

European Journal of Medicinal Chemistry published new progress about Cannabinoid receptor 1 Role: BSU (Biological Study, Unclassified), BIOL (Biological Study). 10305-42-7 belongs to class ethers-buliding-blocks, and the molecular formula is C3H8ClNO2S, Recommanded Product: n-Propylsulphamoyl chloride.

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