Category: 106675-70-1

Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers was written by Otto, Nicola;Opatz, Till. And the article was included in Beilstein Journal of Organic Chemistry in 2012.Application In Synthesis of N1,N2-Dimethoxy-N1,N2-dimethyloxalamide This article mentions the following:

In the search for ligands for the Ullmann diaryl ether synthesis, permitting the coupling of electron-rich aryl bromides at relatively low temperatures, 56 structurally diverse multidentate ligands were screened in a model system that uses copper iodide in acetonitrile with potassium phosphate as the base. The ligands differed largely in their performance, but no privileged structural class could be identified. In the experiment, the researchers used many compounds, for example, N1,N2-Dimethoxy-N1,N2-dimethyloxalamide (cas: 106675-70-1Application In Synthesis of N1,N2-Dimethoxy-N1,N2-dimethyloxalamide).

N1,N2-Dimethoxy-N1,N2-dimethyloxalamide (cas: 106675-70-1) belongs to amides. Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents. Ionic, or saltlike, amides are strongly alkaline compounds ordinarily made by treating ammonia, an amine, or a covalent amide with a reactive metal such as sodium.Application In Synthesis of N1,N2-Dimethoxy-N1,N2-dimethyloxalamide

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

Enantioselective sulfoxide-directed preparation of 1,2-diols from oxalic compounds: formal synthesis of the 10-membered lactone core of ascidiatrienolides and didemnilactones was written by Izzo, Irene;Crumbie, Robin;Solladie, Guy;Hanquet, Gilles. And the article was included in Tetrahedron: Asymmetry in 2005.Synthetic Route of C6H12N2O4 This article mentions the following:

The synthesis of diene I, which is available in both possible absolute configurations is described. This diene constitutes the key intermediate of a previous synthesis of the 10-membered lactone core of the marine natural products ascidiatrienolides and didemnilactones. Intermediate I is available via two successive highly diastereoselective sulfoxide-directed reductions of oxalic diamide II. In the experiment, the researchers used many compounds, for example, N1,N2-Dimethoxy-N1,N2-dimethyloxalamide (cas: 106675-70-1Synthetic Route of C6H12N2O4).

N1,N2-Dimethoxy-N1,N2-dimethyloxalamide (cas: 106675-70-1) belongs to amides. Amides include many other important biological compounds, as well as many drugs like paracetamol, penicillin and LSD. Low-molecular-weight amides, such as dimethylformamide, are common solvents. In simple aromatic amides, fragmentation occurs on both sides of the carbonyl group. If a hydrogen is available in N-substituted aromatic amides, it tends to migrate and form an aromatic amine and the loss of a ketene.Synthetic Route of C6H12N2O4

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 4: Synthesis of N-1 acidic functionality affording analogues with enhanced antiviral activity against HIV was written by Lynch, Christopher L.;Hale, Jeffrey J.;Budhu, Richard J.;Gentry, Amy L.;Mills, Sander G.;Chapman, Kevin T.;MacCoss, Malcolm;Malkowitz, Lorraine;Springer, Martin S.;Gould, Sandra L.;DeMartino, Julie A.;Siciliano, Salvatore J.;Cascieri, Margaret A.;Carella, Anthony;Carver, Gwen;Holmes, Karen;Schleif, William A.;Danzeisen, Renee;Hazuda, Daria;Kessler, Joseph;Lineberger, Janet;Miller, Michael;Emini, Emilio A.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2002.Computed Properties of C6H12N2O4 This article mentions the following:

A series of α-(pyrrolidin-1-yl)acetic acids I [R¹ = H, Me, Me₂CH, cyclopropyl, cyclobutylmethyl, cyclohexyl, Ph, etc.; R² = Ph(CH₂)₃, 4-FC₆H₄; R³ = H, HO] was prepared and investigated as selective and potent antivirals against HIV. Several of the pyrrolidine zwitterions demonstrated reasonable in vitro properties, enhanced antiviral activities and improved pharmacokinetic profiles over the lead pyrrolidine. In the experiment, the researchers used many compounds, for example, N1,N2-Dimethoxy-N1,N2-dimethyloxalamide (cas: 106675-70-1Computed Properties of C6H12N2O4).

N1,N2-Dimethoxy-N1,N2-dimethyloxalamide (cas: 106675-70-1) belongs to amides. The solubilities of amides and esters are roughly comparable. Typically amides are less soluble than comparable amines and carboxylic acids since these compounds can both donate and accept hydrogen bonds. Tertiary amides, with the important exception of N,N-dimethylformamide, exhibit low solubility in water. Amides are stable compounds. The lower-melting members (such as acetamide) can be readily purified by fractional distillation. Most amides are solids which have low solubilities in water.Computed Properties of C6H12N2O4

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics