Gharagheizi, Farhad’s team published research in Industrial & Engineering Chemistry Research in 49 | CAS: 1589-47-5

Industrial & Engineering Chemistry Research published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Name: 2-Methoxypropan-1-ol.

Gharagheizi, Farhad published the artcileA New Neural Network Group Contribution Method for Estimation of Upper Flash Point of Pure Chemicals, Name: 2-Methoxypropan-1-ol, the publication is Industrial & Engineering Chemistry Research (2010), 49(24), 12685-12695, database is CAplus.

A new group contribution-based models is presented to predict the upper flash point temperature of pure compounds based on a large dataset (1294). This neural network model uses several occurrences of 122 chem. groups in a pure compound to predict its related upper flash point limit. The model squared correlation coefficient, average percent error, mean average error, and root-mean-square error over the main dataset (1294 pure compounds) were 0.99, 1.7%, 6, and 8.5, resp.

Industrial & Engineering Chemistry Research published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Name: 2-Methoxypropan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Mortazavi, Saeideh-Sadat’s team published research in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 599 | CAS: 1589-47-5

Colloids and Surfaces, A: Physicochemical and Engineering Aspects published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Name: 2-Methoxypropan-1-ol.

Mortazavi, Saeideh-Sadat published the artcileInfluence of -SO3H groups incorporated as Bronsted acidic parts by tandem post-synthetic functionalization on the catalytic behavior of MIL-101(Cr) MOF for methanolysis of styrene oxide, Name: 2-Methoxypropan-1-ol, the publication is Colloids and Surfaces, A: Physicochemical and Engineering Aspects (2020), 124703, database is CAplus.

Two kinds of Bronsted solid acid catalyst based on MIL-101(Cr) support were prepared by tandem post-synthetic functionalization. Covalent attachment of piperazine and DABCO (DABCO = 1,4 diazabicyclo[2.2.2]octane) followed by reaction with 1,3-propane sultone led to achieving MIL-pip-SO3H and MIL-DABCO-SO3H, resp. The obtained catalysts were characterized using several techniques which confirmed the presence of SO3H groups in the MIL-101(Cr) framework. The catalytic behavior of the functionalized MIL-101(Cr) were evaluated and compared in the methanolysis of styrene oxide. Both solid acid catalysts showed superior catalytic efficiency compared to pristine MIL-101(Cr) under identical reaction conditions due to the presence of SO3H groups, indicating the effect of post-synthetic modification on MIL-101(Cr) MOF.

Colloids and Surfaces, A: Physicochemical and Engineering Aspects published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Name: 2-Methoxypropan-1-ol.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Mortazavi, Saeideh-Sadat’s team published research in Applied Organometallic Chemistry in 34 | CAS: 1589-47-5

Applied Organometallic Chemistry published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Quality Control of 1589-47-5.

Mortazavi, Saeideh-Sadat published the artcileA new Bronsted acid MIL-101(Cr) catalyst by tandem post-functionalization; synthesis and its catalytic application, Quality Control of 1589-47-5, the publication is Applied Organometallic Chemistry (2020), 34(8), e5717, database is CAplus.

A new heterogeneous Bronsted solid acid catalyst was prepared by tandem post-functionalization of MIL-101(Cr) and utilized for acetic acid esterification and alcoholysis of epoxides under solvent-free conditions. First, MIL-101(Cr) was functionalized with pyrazine to achieve MIL-101(Cr)-Pyz. Afterwards, the nucleophilic reaction of MIL-101(Cr)-Pyz with 1,3-propane sultone and next acidification with diluted sulfuric acid gave MIL-101(Cr)-Pyz-RSO3H Bronsted solid acid catalyst. Various characterization methods such as Fourier transformation IR (FT-IR) spectroscopy, X-ray diffraction (XRD), elemental anal. (CHNS), XPS, SEM (SEM), energy-dispersive X-ray (EDX) spectroscopy, thermal anal. (TGA/DTA), acid-base titration, and N2 adsorption/desorption anal. were employed to fully characterize the prepared catalyst. The catalyst showed high activity compared to unmodified MIL-101(Cr) in both catalytic acetic acid esterification and alcoholysis of epoxides. It can also be readily isolated from the reaction mixture and reused three times without major decrease in its activity.

Applied Organometallic Chemistry published new progress about 1589-47-5. 1589-47-5 belongs to ethers-buliding-blocks, auxiliary class Aliphatic hydrocarbon chain,Alcohol,Ether, name is 2-Methoxypropan-1-ol, and the molecular formula is C4H10O2, Quality Control of 1589-47-5.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Ebrahimi, Seyyed Mohammad’s team published research in Research on Chemical Intermediates in 47 | CAS: 6850-57-3

Research on Chemical Intermediates published new progress about 6850-57-3. 6850-57-3 belongs to ethers-buliding-blocks, auxiliary class Amine,Benzene,Ether, name is (2-Methoxyphenyl)methanamine, and the molecular formula is C8H11NO, Computed Properties of 6850-57-3.

Ebrahimi, Seyyed Mohammad published the artcileSynthesis of 2,5-dihydro-3-furans using nano-CoAl2O4, Computed Properties of 6850-57-3, the publication is Research on Chemical Intermediates (2021), 47(8), 3189-3199, database is CAplus.

Nano-CoAl2O4 has been used as an efficient catalyst for the preparation of 5-oxo-2,5-dihydro-3 furancarboxylates by multi-component reaction of phenylglyoxal, di-Me acetylenedicarboxylate and primary amines. The best results were obtained in the presence of 4 mg of nano-CoAl2O4 in CH2Cl2 at room temperature Exptl. simplicity, wide range of products, great yields in concise times, the retrievable of the nanocatalyst and low catalyst loading are some of the substantial features of this method.

Research on Chemical Intermediates published new progress about 6850-57-3. 6850-57-3 belongs to ethers-buliding-blocks, auxiliary class Amine,Benzene,Ether, name is (2-Methoxyphenyl)methanamine, and the molecular formula is C8H11NO, Computed Properties of 6850-57-3.

Referemce:
https://en.wikipedia.org/wiki/Ether,
Ether | (C2H5)2O – PubChem

Zhou, Feng et al. published their research in Organic Letters in 2009 | CAS: 1132669-90-9

5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Safety of 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

Cationic palladium(II)-catalyzed highly enantioselective tandem reactions of ortho-boronate-substituted cinnamic ketones and internal alkynes: a convenient synthesis of optically active indenes. [Erratum to document cited in CA150:329378] was written by Zhou, Feng;Yang, Miao;Lu, Xiyan. And the article was included in Organic Letters in 2009.Safety of 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde The following contents are mentioned in the article:

On page 1406, in Table 1, the equation was incorrectly given; the correct version of the equation is given. This study involved multiple reactions and reactants, such as 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9Safety of 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde).

5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Safety of 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

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

Shen, Qilong et al. published their research in Journal of the American Chemical Society in 2008 | CAS: 562085-85-2

N-(4-Methoxyphenyl)pyridin-3-amine (cas: 562085-85-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Product Details of 562085-85-2

Highly reactive, general and long-lived catalysts for palladium-catalyzed amination of heteroaryl and aryl chlorides, bromides, and iodides: Scope and structure-activity relationships. [Erratum to document cited in CA148:585292] was written by Shen, Qilong;Ogata, Tokutaro;Hartwig, John F.. And the article was included in Journal of the American Chemical Society in 2008.Product Details of 562085-85-2 The following contents are mentioned in the article:

On page 6590, the halogens in the first and second products were incorrectly shown as Br and I, resp. The correct version of the equation is given. This study involved multiple reactions and reactants, such as N-(4-Methoxyphenyl)pyridin-3-amine (cas: 562085-85-2Product Details of 562085-85-2).

N-(4-Methoxyphenyl)pyridin-3-amine (cas: 562085-85-2) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Product Details of 562085-85-2

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

Roy, Amalesh et al. published their research in Tetrahedron Letters in 2007 | CAS: 100927-02-4

4-(Benzyloxy)-3-methylphenol (cas: 100927-02-4) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application In Synthesis of 4-(Benzyloxy)-3-methylphenol

Total synthesis of heliannuol B, an allelochemical from Helianthus annuus was written by Roy, Amalesh;Biswas, Bidyut;Sen, Prabir K.;Venkateswaran, Ramanathapuram V.. And the article was included in Tetrahedron Letters in 2007.Application In Synthesis of 4-(Benzyloxy)-3-methylphenol The following contents are mentioned in the article:

A total synthesis of the allelochem. heliannuol B (I) is described employing ring closing metathesis to generate the central benzoxepane ring system. This study involved multiple reactions and reactants, such as 4-(Benzyloxy)-3-methylphenol (cas: 100927-02-4Application In Synthesis of 4-(Benzyloxy)-3-methylphenol).

4-(Benzyloxy)-3-methylphenol (cas: 100927-02-4) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Application In Synthesis of 4-(Benzyloxy)-3-methylphenol

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

Stille, Julia K. et al. published their research in European Journal of Medicinal Chemistry in 2022 | CAS: 109-85-3

2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Safety of 2-Methoxyethylamine

Design, synthesis and in vitro evaluation of novel SARS-CoV-2 3CLpro covalent inhibitors was written by Stille, Julia K.;Tjutrins, Jevgenijs;Wang, Guanyu;Venegas, Felipe A.;Hennecker, Christopher;Rueda, Andres M.;Sharon, Itai;Blaine, Nicole;Miron, Caitlin E.;Pinus, Sharon;Labarre, Anne;Plescia, Jessica;Burai Patrascu, Mihai;Zhang, Xiaocong;Wahba, Alexander S.;Vlaho, Danielle;Huot, Mitchell J.;Schmeing, T. Martin;Mittermaier, Anthony K.;Moitessier, Nicolas. And the article was included in European Journal of Medicinal Chemistry in 2022.Safety of 2-Methoxyethylamine The following contents are mentioned in the article:

Efforts in the design and synthesis of submicromolar covalent inhibitors when the enzymic activity of the viral protease was used as a screening platform were reported. This study involved multiple reactions and reactants, such as 2-Methoxyethylamine (cas: 109-85-3Safety of 2-Methoxyethylamine).

2-Methoxyethylamine (cas: 109-85-3) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Safety of 2-Methoxyethylamine

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

Matsuda, Takanori et al. published their research in Synlett in 2015 | CAS: 1132669-90-9

5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Electric Literature of C14H19BO4

Rhodium-Catalyzed Addition-Spirocyclization of Arylboronic Esters Containing β-Aryl α,β-Unsaturated Ester Moiety was written by Matsuda, Takanori;Yasuoka, Satoshi;Watanuki, Shoichi;Fukuhara, Keisuke. And the article was included in Synlett in 2015.Electric Literature of C14H19BO4 The following contents are mentioned in the article:

In this study, we developed a rhodium(I)-catalyzed spirocyclization. The reaction includes 1,4-rhodium migration and provides a route for forming spirocyclic 1-indanones. This study involved multiple reactions and reactants, such as 5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9Electric Literature of C14H19BO4).

5-Methoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (cas: 1132669-90-9) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Electric Literature of C14H19BO4

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

Reinisch, Jens et al. published their research in Industrial & Engineering Chemistry Research in 2016 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.SDS of cas: 112-59-4

Correction to “Predicting Flash Points of Pure Compounds and Mixtures with COSMO-RS” [Erratum to document cited in CA164:106271] was written by Reinisch, Jens;Klamt, Andreas. And the article was included in Industrial & Engineering Chemistry Research in 2016.SDS of cas: 112-59-4 The following contents are mentioned in the article:

The final conversion within eq 4 in the original manuscript is incorrect; The correct equation has been given. There is an analog error in eq 11; The corrected equation has been given. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4SDS of cas: 112-59-4).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.SDS of cas: 112-59-4

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