Doobary, Sayad’s team published research in Journal of Organic Chemistry in 86 | CAS: 33697-81-3

Journal of Organic Chemistry published new progress about 33697-81-3. 33697-81-3 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Carboxylic acid,Benzene,Phenol, name is 3-Chloro-4-hydroxyphenylacetic acid, and the molecular formula is C8H7ClO3, COA of Formula: C8H7ClO3.

Doobary, Sayad published the artcileIntramolecular Alkene Fluoroarylation of Phenolic Ethers enabled by Electrochemically Generated Iodane, COA of Formula: C8H7ClO3, the publication is Journal of Organic Chemistry (2021), 86(22), 16095-16103, database is CAplus and MEDLINE.

Herein, synthesis of 3-fluorinated chromanes from allylic phenol ethers was described. Oxidant-free approach takes advantage of an electrochem. generation of a hypervalent iodine species, difluoro-λ3-tolyl iodane, which mediates the alkene fluoroarylation. High yields and selectivity for this transformation are achieved for electron poor substrates. The redox chem. has been characterized for the electrochem. generation of the iodane in the presence of fluoride, and insights into the mechanism are given. The transformation has been demonstrated on larger gram scales, which represents the potential broader utility of the process.

Journal of Organic Chemistry published new progress about 33697-81-3. 33697-81-3 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Carboxylic acid,Benzene,Phenol, name is 3-Chloro-4-hydroxyphenylacetic acid, and the molecular formula is C8H7ClO3, COA of Formula: C8H7ClO3.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Nongmaithem, Sapana’s team published research in Journal of Plant Growth Regulation in 40 | CAS: 33697-81-3

Journal of Plant Growth Regulation published new progress about 33697-81-3. 33697-81-3 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Carboxylic acid,Benzene,Phenol, name is 3-Chloro-4-hydroxyphenylacetic acid, and the molecular formula is C8H7ClO3, Safety of 3-Chloro-4-hydroxyphenylacetic acid.

Nongmaithem, Sapana published the artcileEnhanced Polar Auxin Transport in Tomato Polycotyledon Mutant Seems to be Related to Glutathione Levels, Safety of 3-Chloro-4-hydroxyphenylacetic acid, the publication is Journal of Plant Growth Regulation (2021), 40(2), 761-773, database is CAplus.

Glutathione-dependent root growth in Arabidopsis is linked to polar auxin transport (PAT). Arabidopsis mutants with reduced glutathione (GSH) levels also show reduced PAT. To gain an insight into the relationship between PAT and GSH level, we analyzed tomato polycotyledon mutant, pct1-2, which has enhanced PAT. Microarray anal. of gene expression in pct1-2 mutant revealed underexpression of several genes related to glutamate and glutathione metabolism In consonance with microarray anal., enzymic as well as in vivo assay revealed higher glutathione levels in the early phase of pct1-2 seedling growth than WT. The inhibition of auxin transport by 2,3,5-triiodobenzoic acid (TIBA) reduced both GSH level and PIN1 expression in pct1-2 root tips. The reduction of in vivo GSH accumulation in pct1-2 root tips by buthionine sulfoximine (BSO) stimulated elongation of the short root of pct1-2 mutant akin to TIBA. The rescue of the short root phenotype of the pct1-2 mutant was restricted to TIBA and BSO. The other auxin transport inhibitors 1-N-naphthylphthalamic acid (NPA), 2-[4-(diethylamino)-2-hydroxybenzoyl] benzoic acid (BUM), 3-chloro-4-hydroxyphenylacetic acid (CHPAA), brefeldin and gravacin inhibited root elongation in both WT and pct1-2 mutant. Our results indicate a relationship between PAT and GSH levels in tomato akin to Arabidopsis. Our work also highlights that TIBA rescues the short root phenotype of the pct1-2 mutant by acting on a PAT component distinct from the site of action of other PAT inhibitors.

Journal of Plant Growth Regulation published new progress about 33697-81-3. 33697-81-3 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Carboxylic acid,Benzene,Phenol, name is 3-Chloro-4-hydroxyphenylacetic acid, and the molecular formula is C8H7ClO3, Safety of 3-Chloro-4-hydroxyphenylacetic acid.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Belyakova, Z. V.’s team published research in Russian Journal of General Chemistry in 80 | CAS: 14799-93-0

Russian Journal of General Chemistry published new progress about 14799-93-0. 14799-93-0 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is Dichloro(methyl)(octyl)silane, and the molecular formula is C9H20Cl2Si, Name: Dichloro(methyl)(octyl)silane.

Belyakova, Z. V. published the artcileEffect of catalysts on the reaction of allyl esters with hydrosilanes, Name: Dichloro(methyl)(octyl)silane, the publication is Russian Journal of General Chemistry (2010), 80(4), 728-733, database is CAplus.

Hydrosilylation of allyl esters XOCH2CH:CH2 (X = MeCO, CF3CO, C3F7CO, CH2:C(Me)CO), PhOCH2CH:CH2 and ClCH2CH:CH2 with hydrosilanes HSiCl3, HSi(OEt)3 and HSiMeCl2 in the presence of Speier’s catalyst, Speier’s catalyst with additives, and of various Ni compounds was studied. The catalytic hydrosilylation reaction in the presence of the Speier catalyst is accompanied by reductions Additives to the Speier catalyst (vinyltriethoxysilane, allyl acetate and trifluoroacetate) suppress the reduction reaction considerably. E.g., hydrosilylation of allyl methacrylate with HSiCl3 in the presence of Speier’s catalyst gave CH2:C(Me)CO2CH2CH2CH2SiCl3 in 67% yield and a ratio of 5.55 of the addition product to the reduction product. The same reaction in the presence of Speier’s catalyst and vinyltriethoxysilane afforded CH2:C(Me)CO2CH2CH2CH2SiCl3 in 87% yield and a ratio of 114.1 of the addition product to the reduction product. In the presence of the studied Ni compounds mainly reduction and isomerization reactions of allyl Ph ether occurred. The best Ni catalysts for hydrosilylation were mixtures of NiCl2 or Ni(acac)2 with phosphine oxides. In contrast to allyl Ph ether, the hydrosilylation of simple olefins proceeds easier. E.g., hydrosilylation of 1-heptene with HSiCl3 in the presence of NiCl2 and (octyl)3P:O gives the hydrosilylation product trichloroheptylsilane in 94% yield in the reaction mixture

Russian Journal of General Chemistry published new progress about 14799-93-0. 14799-93-0 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is Dichloro(methyl)(octyl)silane, and the molecular formula is C9H20Cl2Si, Name: Dichloro(methyl)(octyl)silane.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Brzozowski, Zdzislaw’s team published research in Acta Poloniae Pharmaceutica in 50 | CAS: 4584-49-0

Acta Poloniae Pharmaceutica published new progress about 4584-49-0. 4584-49-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Salt,Amine,Aliphatic hydrocarbon chain, name is 2-Chloro-N,N-dimethylpropan-1-amine hydrochloride, and the molecular formula is C5H13Cl2N, COA of Formula: C5H13Cl2N.

Brzozowski, Zdzislaw published the artcileDerivatives of 2-mercaptobenzenesulfonamide. XIII. Syntheses and some pharmacological properties of 1-[4-chloro-2-(dialkylaminoalkylthio)-5-methylbenzenesulfonyl]-2-imidazolidinone hydrochlorides, COA of Formula: C5H13Cl2N, the publication is Acta Poloniae Pharmaceutica (1993), 50(4-5), 359-64, database is CAplus and MEDLINE.

In the search for new antiarrhythmic agents, 3-[(4-chloro-2-mercapto-5-methylphenyl)sulfonyl]imidazolidinone I (R = H) was treated with dialkylaminoalkyl chloride hydrochlorides in Me2CHONa-Me2CHOH to yield I (R = Me2NCH2CHMe, Me2NCMe2CH2, and R1CH2CH2; R1 = Pr2N, Bu2N, (C6H11)2N, piperidinyl, 2,6-dimethylpiperidinyl, morpholinyl, and piperazinyl). Data for LD50 and activity against acinitine- and BaCl2-induced arrhythmia in rats are presented for I hydrochlorides.

Acta Poloniae Pharmaceutica published new progress about 4584-49-0. 4584-49-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Salt,Amine,Aliphatic hydrocarbon chain, name is 2-Chloro-N,N-dimethylpropan-1-amine hydrochloride, and the molecular formula is C5H13Cl2N, COA of Formula: C5H13Cl2N.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Eremeev, A. V.’s team published research in Khimiya Geterotsiklicheskikh Soedinenii in | CAS: 18791-02-1

Khimiya Geterotsiklicheskikh Soedinenii published new progress about 18791-02-1. 18791-02-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 2,3-Dibromopropionylchloride, and the molecular formula is C3H3Br2ClO, Computed Properties of 18791-02-1.

Eremeev, A. V. published the artcileAsymmetric unbridged nitrogen. 37. Absolute configuration of diastereomeric derivatives of N-substituted aziridine-2-carboxylic acids, Computed Properties of 18791-02-1, the publication is Khimiya Geterotsiklicheskikh Soedinenii (1984), 1343-8, database is CAplus.

Both (R,S)- and (S,S)-aziridinecarboxanilides (I; R, R1 = Me, H; Me, Br; CHMe2, Br) were prepared and the diastereoisomers distinguished by their 1H and 15N NMR and CD spectra.

Khimiya Geterotsiklicheskikh Soedinenii published new progress about 18791-02-1. 18791-02-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 2,3-Dibromopropionylchloride, and the molecular formula is C3H3Br2ClO, Computed Properties of 18791-02-1.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Gosset, Antoine’s team published research in International Journal of Hygiene and Environmental Health in 224 | CAS: 637-07-0

International Journal of Hygiene and Environmental Health published new progress about 637-07-0. 637-07-0 belongs to chlorides-buliding-blocks, auxiliary class Inhibitor,Cell Cycle,PPAR, name is Ethyl 2-(4-chlorophenoxy)-2-methylpropanoate, and the molecular formula is C12H15ClO3, Recommanded Product: Ethyl 2-(4-chlorophenoxy)-2-methylpropanoate.

Gosset, Antoine published the artcileEcotoxicological risk assessment of micropollutants from treated urban wastewater effluents for watercourses at a territorial scale: Application and comparison of two approaches, Recommanded Product: Ethyl 2-(4-chlorophenoxy)-2-methylpropanoate, the publication is International Journal of Hygiene and Environmental Health (2020), 113437, database is CAplus and MEDLINE.

In most cases, urban Wastewater Treatment Plants (WWTP) only partially abate pollutants occurring in the influent. Treated effluents can thus contain a complex mixture of ecotoxic pollutants, such as heavy metals, detergents, disinfectants, plasticizers, pharmaceuticals residues or pesticides. In this context, Ecotoxicol. Risk Assessment (ERA) provide essential decision-making tools to public authorities for establishing environmental policies and conducting territorial planning. The present work aims to develop a territorial-scale ERA methodol. using two complementary approaches based on a Risk Quotient (RQ) calculation: (1) the first, based on the risk linked to each individual pollutant (single substances ERA); (2) the second, considering all pollutants present, and the “cocktail effect” (mixture ERA). This research was performed at 33 urban WWTPs of in a highly urbanized part of France (Lyon area). Initial min., median and maximum pollutant concentrations in treated effluents were obtained from a literature review of physico-chem. anal. studies, to reconstitute “typical” effluents. The classical approach (single substances ERA) identified the riskiest substances (e.g. endocrine disruptors, as the Estrone with RQ up to 593.75), and showed the risks for each WWTP. The mixture ERA approach revealed new risks, which were not highlighted in the classical ERA approach, thus increasing the number of WWTPs identified as at risk. This study shows the importance of accounting for the cocktail effect, which is not considered in current regulatory decisions. Finally, this methodol. allowed us to identify the riskiest situations (often medium sized WWTPs, releasing into small streams), that could worsen in the context of climate change.

International Journal of Hygiene and Environmental Health published new progress about 637-07-0. 637-07-0 belongs to chlorides-buliding-blocks, auxiliary class Inhibitor,Cell Cycle,PPAR, name is Ethyl 2-(4-chlorophenoxy)-2-methylpropanoate, and the molecular formula is C12H15ClO3, Recommanded Product: Ethyl 2-(4-chlorophenoxy)-2-methylpropanoate.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Proevska, L. I.’s team published research in Dyes and Pigments in 36 | CAS: 4569-86-2

Dyes and Pigments published new progress about 4569-86-2. 4569-86-2 belongs to chlorides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Benzene, name is 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride, and the molecular formula is C22H23ClN4, HPLC of Formula: 4569-86-2.

Proevska, L. I. published the artcile1H NMR spectra and structure of safranines. Hindered rotation of the 3-dialkylamino group in 7-azo derivatives, HPLC of Formula: 4569-86-2, the publication is Dyes and Pigments (1998), 36(2), 177-190, database is CAplus.

The 1H NMR spectra of safranine derivatives are reported. Semiempirical calculations indicate that the high shielding of the 4- and 6-proton adjacent to an amino or hydroxyl group (resonating between 5.5 and 6.0 ppm) is due to accumulation of neg. charge on the 4-and 6-C atoms, augmented by the magnetic anisotropy effect of the orthogonal 5-Ph ring. The ortho protons of the latter resonate up field to the meta and para protons. Hindered rotation of dialkylamino groups, altogether unexpected in view of the rather low barriers in similar anilines, is observed only in the azo derivatives AM1 suggests that this is due to destabilization of the transition state when an amino group is substituted for an azo group.

Dyes and Pigments published new progress about 4569-86-2. 4569-86-2 belongs to chlorides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Benzene, name is 3-Amino-7-(diethylamino)-5-phenylphenazin-5-ium chloride, and the molecular formula is C22H23ClN4, HPLC of Formula: 4569-86-2.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Nevalainen, Vesa’s team published research in Journal of Chemical Research, Synopses in | CAS: 1002-41-1

Journal of Chemical Research, Synopses published new progress about 1002-41-1. 1002-41-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 1,2-Bis(2-chloroethyl)disulfane, and the molecular formula is C4H8Cl2S2, Computed Properties of 1002-41-1.

Nevalainen, Vesa published the artcileStudies on the formation of dihydro-1,4-oxathiines by halogenation of 1,3-oxathiolanes, Computed Properties of 1002-41-1, the publication is Journal of Chemical Research, Synopses (1988), 182-3, database is CAplus.

Dihydro-1,4-oxathiins I (R, R1 = Me, H; Et, H; Ph, H; Me, Ph; CO2Me, H; Me, CO2Me; Me, CONHPh) were prepared in 6-45% yields by the halogenation of the resp. 1,3-oxathiolanes II (R, R1 = Me, H; Me, Me; Ph, H; Me, Ph; CO2Me, H; Me, CO2Me; Me, CONHPh) with SOCl2. Several byproducts were formed.

Journal of Chemical Research, Synopses published new progress about 1002-41-1. 1002-41-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 1,2-Bis(2-chloroethyl)disulfane, and the molecular formula is C4H8Cl2S2, Computed Properties of 1002-41-1.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Nevalainen, Vesa’s team published research in Acta Chemica Scandinavica in 44 | CAS: 1002-41-1

Acta Chemica Scandinavica published new progress about 1002-41-1. 1002-41-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 1,2-Bis(2-chloroethyl)disulfane, and the molecular formula is C4H8Cl2S2, COA of Formula: C4H8Cl2S2.

Nevalainen, Vesa published the artcileStudies on the preparation of dihydro-1,4-oxathiines. Computer-assisted evaluation of the results of retrosynthetic analysis verified by synthetic experiments and by-product analyses. Synthetic pathways involving α-sulfenylated ketones and 1,3-oxathiolanes of α-halo and α-hydroxy ketones, COA of Formula: C4H8Cl2S2, the publication is Acta Chemica Scandinavica (1990), 44(6), 591-602, database is CAplus.

The preparation of 2- and 2,3-substituted 5,6-dihydro-1,4-oxathiines (I, R = Me or Ph, R1 = H, Me, CO2H, CO2Me, CO2Et, or CONHPh) was studied by computer simulation and by experiment Three major synthetic pathways, involving 2-(1-hydroxyalkyl)-1,3-oxathiolanes, 2-(1-haloalkyl)-1,3-oxathiolanes, 2-hydroxyethylthiomethyl ketones, methanesulfonates of 2-hydroxyethylthiomethyl ketones and 2-chloroethylthiomethyl ketones as intermediates, were evaluated, by running the program CAMEO, and by experiment The results of the two approaches were compared and the major byproducts of the reactions were identified by GLC/MS.

Acta Chemica Scandinavica published new progress about 1002-41-1. 1002-41-1 belongs to chlorides-buliding-blocks, auxiliary class Aliphatic Chain, name is 1,2-Bis(2-chloroethyl)disulfane, and the molecular formula is C4H8Cl2S2, COA of Formula: C4H8Cl2S2.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Kovtun, E. A.’s team published research in Fibre Chemistry (Translation of Khimicheskie Volokna) in 32 | CAS: 38146-42-8

Fibre Chemistry (Translation of Khimicheskie Volokna) published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, SDS of cas: 38146-42-8.

Kovtun, E. A. published the artcileCreation of sutures with antimicrobial properties, SDS of cas: 38146-42-8, the publication is Fibre Chemistry (Translation of Khimicheskie Volokna) (2000), 32(4), 287-292, database is CAplus.

It was found that decamethoxin, as a broad-spectrum antiseptic with a pronounced antibacterial and fungicidal action, and BF-6 phenol-polyvinylacetal adhesive, which gives complex sutures the structure of a pseudomonofilament, are best as antimicrobial additives in a modifying composite for giving surgical sutures antimicrobial properties. A decamethoxin content in the modifying composite of 10% of the weight of BF-6 (1.7-2.0% in the suture) is sufficient for manifestation of the antimicrobial effect with respect to Staphylococcus aureus, E. coli, and yeast-like fungi. The antimicrobial activity of a suture with a 1.7-2.0 weight % decamethoxin content in the period from 2 to 24 h increases by 4 times with respect to E. coli and by 8 times with respect to Staphylococcus aureus and yeast-like fungi. Application of a coating of BF-6 adhesive with decamethoxin has almost no effect on the physicomech. properties of the sutures, but the capillarity decreases significantly (by ∼86%), which also decreases the probability of wound infection. The kinetics of release of decamethoxin does not change after radiation sterilization of the sutures, i.e., the composition and content of the antimicrobial additive in the modified sutures and its antimicrobial activity are preserved. The optimum medium for storage of sterile modified sutures is 1% decamethoxin solution After 12 days of storage, the sutures remain sterile and lose a maximum of 6% of the breaking strength.

Fibre Chemistry (Translation of Khimicheskie Volokna) published new progress about 38146-42-8. 38146-42-8 belongs to chlorides-buliding-blocks, auxiliary class Achiral Phase-Transfer Catalysts, name is N1,N10-Bis(2-((2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoethyl)-N1,N1,N10,N10-tetramethyldecane-1,10-diaminium chloride, and the molecular formula is C38H74Cl2N2O4, SDS of cas: 38146-42-8.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics