Tag: M.W=0-100

An article Iridium-catalysed C-H borylation of beta-aryl-aminopropionic acids WOS:000565016900013 published article about PURE LITHIUM AMIDES; AMMONIA EQUIVALENTS; CONJUGATE ADDITION; AMINO-ACIDS; IN-VITRO; MECHANISM; DERIVATIVES; ANTAGONISTS; ACTIVATION; INHIBITORS in [Robinson, Henry; Stillibrand, Joe; Simelis, Klemensas; Nortcliffe, Andrew] Univ Nottingham, Sch Chem, GlaxoSmithKline Carbon Neutral Labs Sustainable C, Triumph Rd, Nottingham NG7 2TU, England; [Macdonald, Simon J. F.] GlaxoSmithKline, Med Res Ctr, Gunnels Wood Rd, Stevenage SG1 2NY, Herts, England in 2020.0, Cited 29.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. Recommanded Product: 67-51-6

Iridium-catalysed catalytic, regioselective C-H borylation of beta-aryl-aminopropionic acid derivatives gives access to 3,5-functionalised protected beta-aryl-aminopropionic acid boronates. The synthetic versatility of these new boronates is demonstrated through sequential one-pot functionalisation reactions to give diverse building blocks for medicinal chemistry. The C-H borylation is also effective for dipeptide substrates. We have exemplified this methodology in the synthesis of a pan alpha(v)integrin antagonist.

About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Robinson, H; Stillibrand, J; Simelis, K; Macdonald, SJF; Nortcliffe, A or concate me.. Recommanded Product: 67-51-6

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Quality Control of 3,5-Dimethyl-1H-pyrazole. Authors Saju, A; Mondal, A; Chattopadhyay, T; Kolliyedath, G; Kundu, S in AMER CHEMICAL SOC published article about in [Saju, Ananya; Mondal, Aditesh; Chattopadhyay, Taraknath; Kolliyedath, Gayathri; Kundu, Subrata] Indian Inst Sci Educ & Res Thiruvananthapuram IIS, Sch Chem, Thiruvananthapuram 695551, Kerala, India in 2020.0, Cited 37.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6

The controlled generation of hydrogen sulfide (H2S) under biologically relevant conditions is of paramount importance due to therapeutic interests. Via exploring the reactivity of a structurally characterized phenolate-bridged dinuclear zinc(II)-aqua complex {LZnII(OH2)}(2)(ClO4)(2) (1a) as a hydrolase model, we illustrate in this report that complex 1a readily hydrolyses CS2 in the presence of Et3N to afford H2S. In contrast, penta-coordinated [Zn-II] sites in dinuclear {(LZnII)(2)(mu-X)}(ClO4) complexes (7, X = OAc; 8, X = dimethylpyrazolyl) do not mediate CS2 hydrolysis in the presence of externally added water and Et3N presumably due to the unavailability of a coordination site for water at the [Zn-II] centers. Moreover, [Zn-II]-OH sites present in the isolated tetranuclear zinc(II) complex {(LZnII)(2)(mu-OH)}(2)(ClO4)(2) (4) react with CS2, thereby suggesting that the [Zn-II]-OH site serves as the active nucleophile. Furthermore, mass spectrometric analyses on the reaction mixture consisting of 1a/Et3N and CS2 suggest the involvement of zinc(II)-thiocarbonate (3a) and COS species, thereby providing mechanistic insights into CS2 hydrolysis mediated by the dinuclear [Zn-II] hydrolase model complex 1a.

Quality Control of 3,5-Dimethyl-1H-pyrazole. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Saju, A; Mondal, A; Chattopadhyay, T; Kolliyedath, G; Kundu, S or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

An article Synthesis of 1,3,5-Trisubstituted Pyrazoles and Hydrazones Using Fe3O4@CeO2 Nanocomposite as an Efficient Heterogeneous Nanocatalyst WOS:000527931800018 published article about ACID; CATALYST; OXIDE in [Hassani, H.; Jahani, Z.] Payame Noor Univ, Dept Chem, Tehran 193954697, Iran in 2020.0, Cited 32.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. Recommanded Product: 3,5-Dimethyl-1H-pyrazole

Pyrazoles and hydrazones, as two significant kinds of potentially bioactive compounds, were produced with good to excellent yields by condensation of beta-dicarbonyl compounds with hydrazines in aqueous media in the presence of Fe3O4@CeO2 nanocomposite as an efficient heterogeneous nanocatalyst. The magnetic nanocatalyst can readily be separated using an external magnet and reused at least six times without significant loss in activity. The products were characterized by IR and H-1 and(13)C NMR spectra.

Recommanded Product: 3,5-Dimethyl-1H-pyrazole. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Hassani, H; Jahani, Z or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

HPLC of Formula: C5H8N2. Recently I am researching about ONE-POT SYNTHESIS; ASYMMETRIC CONJUGATE ADDITION; MICHAEL ADDITION; ELECTRON-DEFICIENT; ENANTIOSELECTIVE SYNTHESIS; NUCLEOPHILIC-ADDITION; AROMATIC-AMINES; H BONDS; N-H; COMPLEXES, Saw an article supported by the National Research Foundation of Korea (NRF)National Research Foundation of Korea [NRF-2017R1A2B4008310]; Korean government (MSIP) [NRF-2015M3A9E6029594]; Kwangwoon University; Bio & Medical Technology Development Program of the National Research Foundation (NRF); Korean government (MOHW)Korean Government [NRF-2015M3A9E6029594]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Park, S; Lee, H; Lee, Y. The CAS is 67-51-6. Through research, I have a further understanding and discovery of 3,5-Dimethyl-1H-pyrazole

An efficient and straightforward method for the synthesis of new and versatile sulfonyl-functionalized allylic amines through the selective copper-catalyzed aza-1,6-conjugate addition of heterocycles or arylamines to 1,4-disubstituted-1,3-dienyl sulfones has been developed. This catalytic process is promoted by a combination of an easily prepared and sterically demanding N-heterocyclic carbene-based copper complex and KOt-Bu under mild reaction conditions to provide a broad range of (E)-allylic amines with excellent regio- and stereoselectivities.

About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Park, S; Lee, H; Lee, Y or concate me.. HPLC of Formula: C5H8N2

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Quality Control of 3,5-Dimethyl-1H-pyrazole. In 2020.0 J ADHES SCI TECHNOL published article about SOL-GEL COATINGS; MILD-STEEL; DERIVATIVES; ACID; PROTECTION in [Masoumi, Asad; Hossaini Sadr, Moayad; Soltani, Behzad] Azarbaijan Shahid Madani Univ, Dept Chem, Fac Sci, Tabriz, Iran in 2020.0, Cited 33.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6.

A series of pyrazole ligands named as 1,4-bis(3,5-dimethylpyrazol-1-yl)butane (bbd), 1,3-bis(3,5-dimethylpyrazol-1-yl)propane (bdpp), and 1,3-bis(3,5-dimethylpyrazol-1-yl)propane-2-ol (bdpo) along with their transition metal complexes including [Cu-2(mu(3)-SCN)(2)(mu-bbd)](n), [Cu-2(mu(3)-SCN)(2)(mu-bdpp)](n), and [Cu2Hg(mu(2)-SCN)(2)(bdpo)(2)(CH3COO)(2)](n)were synthesized and characterized using FT-IR and Uv-vis spectroscopies, as well as thermal gravimetric analysis. The prepared compounds were investigated as corrosion inhibitors to protect mild steel in 0.5 M H(2)SO(4)solution. Corrosion tests were performed by electrochemical impedance spectroscopy and potentiodynamic polarization measurements. The pyrazole ligands exhibited inhibition efficiencies in a range of 38-78%, which introduced them as moderate inhibitors. On the other hand, the pyrazole complexes showed inhibition efficiencies higher than 85%, demonstrating their high potentials to mitigate the steel corrosion. In addition, the bimetallic complex resulted in higher corrosion resistance than the two monometallic complexes. This was evidence of a critical role of the coordinated metal of the complex in forming an adhesive protection film on the steel surface.

Quality Control of 3,5-Dimethyl-1H-pyrazole. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Masoumi, A; Sadr, MH; Soltani, B or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Authors Fu, X; Hao, Y; Bai, HY; Duan, AB; Zhang, SY in AMER CHEMICAL SOC published article about ASYMMETRIC ALPHA-AMINATION; VINYLOGOUS ALDOL REACTION; ELECTROPHILIC AMINATION; HIGHLY REGIO; KETONES; ACCESS; ENALS; BONDS in [Fu, Xin; Duan, Abing] Hunan Univ, Coll Environm Sci & Technol, Changsha 410082, Peoples R China; [Fu, Xin; Hao, Yu; Bai, He-Yuan; Zhang, Shu-Yu] Shanghai Jiao Tong Univ, Key Lab Thin Film & Microfabricat Technol, Minist Educ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China; [Fu, Xin; Hao, Yu; Bai, He-Yuan; Zhang, Shu-Yu] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, Shanghai 200240, Peoples R China in 2021.0, Cited 62.0. COA of Formula: C5H8N2. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6

A cobalt-catalyzed regio- and enantioselective gamma-amination of beta,gamma-unsaturated N-acylpyrazoles that delivers the corresponding gamma-amination products in good regio- and enantioselectivity has been established. Moreover, the nitrogen-containing compounds could be easily synthesized. DFT calculations have been provided to explain regio- and enantioselectivity for this gamma-amination. The chiral gamma-amination products were readily converted into the chiral gamma-amino acid derivatives.

COA of Formula: C5H8N2. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Fu, X; Hao, Y; Bai, HY; Duan, AB; Zhang, SY or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

In 2020.0 ORG LETT published article about ALPHA-AMINO-ACIDS; DECARBOXYLATIVE ARYLATION; 4+2 CYCLOADDITIONS; AZOMETHINE YLIDES; MICHAEL ADDITION; CASCADE REACTION; 3-NITROINDOLES; ACCESS; FUNCTIONALIZATION; PYRROLOINDOLINES in [Huang, Xu-Lun; Cheng, Yuan-Zheng; Zhang, Xiao; You, Shu-Li] Chinese Acad Sci, Univ Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai Inst Organ Chem,Ctr Excellence Mol Synth, Shanghai 200032, Peoples R China; [Huang, Xu-Lun; You, Shu-Li] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China; [Zhang, Xiao] Fujian Normal Univ, Coll Chem & Mat Sci, Fujian Key Lab Polymer Sci, Fujian Prov Key Lab Adv Mat Oriented Chem Engn, Fuzhou 350007, Peoples R China in 2020.0, Cited 119.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. Product Details of 67-51-6

Dearomatization of indole derivatives offers a straightforward approach to access diverse indolines. To date, the corresponding dearomative transformations involving electron-deficient indoles are limited. Herein, we report a one-electron strategy for dearomatization of electron-deficient indoles via a photoredox-catalyzed hydroalkylation employing commercially available glycine derivatives as the hydrofunctionalization reagents. Followed by DBU-mediated lactamization, structurally appealing lactam-fused indolines are obtained in good to excellent yields with exclusive selectivity.

Product Details of 67-51-6. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Huang, XL; Cheng, YZ; Zhang, X; You, SL or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

In 2020.0 TRANSIT METAL CHEM published article about RHODIUM; LIGANDS; ALKENES in [Gamede, Noluthando V.; Kapfunde, Tsitsi A.; Ocansey, Edward; Ngumbu, Denis M.; Darkwa, James; Makhubela, Banothile C. E.] Univ Johannesburg, Dept Chem, POB 524, ZA-2006 Auckland Pk, South Africa in 2020.0, Cited 21.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. SDS of cas: 67-51-6

The industrial process of hydroformylation or the oxo process has been used for many years in the production of aldehydes from alkenes. Different metals have been used as efficient catalysts for hydroformylation, in which linear and branched aldehydes are the products obtained; therefore, the development of new catalysts for hydroformylation with high selectivity to aldehydes is important. Rhodium complexes 6-9 were synthesized using [RhCl(CO)(2)](2), or [RhCl(COD)](2), with either pyrazolylpyridyl N ‘ N ‘ N pincer ligands or a pyrazolylpyridyl N ‘ N ligand. These complexes were then evaluated as catalyst precursors in the hydroformylation reaction using a variety of alkenes. The catalysts all showed activity in hydroformylation but the most active catalyst was methyl-substituted pyrazolyl-rhodium complex 7 following optimization of temperature, syngas pressure and amount of catalyst. Other olefinic substrates were used for hydroformylation in the presence of 7 under the optimum hydroformylation conditions. Undecene and dodecene as substrates only showed minimal formation of aldehydes with predominantly isomerization of the alkene being observed.

SDS of cas: 67-51-6. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Gamede, NV; Kapfunde, TA; Ocansey, E; Ngumbu, DM; Darkwa, J; Makhubela, BCE or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

In 2021.0 J ORG CHEM published article about REGIOSELECTIVE IODINATION; NITROSYLSULFURIC ACID; AROMATIC-COMPOUNDS; EFFICIENT METHOD; NITROGEN-OXIDE; C-13 NMR; MILD; CONVENIENT; BROMINATION; 3,5-DIARYLISOXAZOLES in [Bondarenko, Oksana B.; Karetnikov, Georgy L.; Komarov, Arseniy, I; Pavlov, Aleksandr, I; Nikolaeva, Svetlana N.] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia in 2021.0, Cited 58.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6. HPLC of Formula: C5H8N2

A new convenient and versatile halogenating system (R(4)NHal/NOHSO4), giving straightforward and general access to halogenated 3,5-diaryl- and alkylarylisoxazoles, pyrazoles and electron-rich benzenes from the corresponding scaffolds, is suggested. The method provides excellent regioselectivity, scalability to the gram scale, and a broad scope for both aromatics and halogens. A three-step, one-pot reaction protocol was developed, and a series of 3,5-diaryl-4-haloisoxazoles has been efficiently synthesized from 1,2-diarylcyclopropanes under suggested nitrosating-halogenating conditions.

HPLC of Formula: C5H8N2. About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Bondarenko, OB; Karetnikov, GL; Komarov, AI; Pavlov, AI; Nikolaeva, SN or concate me.

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics

Authors Yuan, Y; Xu, RJ; Zhao, HK in ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD published article about in [Yuan, Yang; Zhao, Hongkun] Yangzhou Univ, Coll Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China; [Xu, Renjie] Yangzhou Univ, Guangling Coll, Yangzhou 225009, Jiangsu, Peoples R China in 2019.0, Cited 1.0. Quality Control of 3,5-Dimethyl-1H-pyrazole. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6

Errors were discovered regarding the published equation coefficients of Yao and co-workers (2017) for mathematically describing the solubility of 3,5-dimethylpyrazole in nine organic solvents using the NRTL model. Larger differences were found between our back-calculated data and those reported in the authors’ published paper. The equation parameters were re-regressed based on the reported solubility data. (C) 2018 Elsevier Ltd.

About 3,5-Dimethyl-1H-pyrazole, If you have any questions, you can contact Yuan, Y; Xu, RJ; Zhao, HK or concate me.. Quality Control of 3,5-Dimethyl-1H-pyrazole

Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics