Category: 737-31-5

In an article, author is Kovalev, V. V., once mentioned the application of 737-31-5, HPLC of Formula: https://www.ambeed.com/products/737-31-5.html, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, molecular formula is C11H8I3N2NaO4, molecular weight is 635.8954, MDL number is MFCD00051544, category is phthalazine. Now introduce a scientific discovery about this category.

The coordination compound [ZnCl2(Phtz)(2)] has been synthesized by the reaction of ZnCl2 with phthalazine (Phtz, L, C8H6N2) in an ethanol solution. Its crystal structure has been determined: crystals are triclinic, space group P 0000000, a = 7.346(1) , b = 8.095(1) , c = 14.275(1) , alpha = 85.63(1)A degrees, beta = 75.75(1)A degrees, gamma = 88.43(1)A degrees, V = 820.4(2) (3), rho(calc) = 1.605 g/cm(3), Z = 2. The zinc atom is tetrahedrally coordinated to two crystallographically nonequivalent chlorine atoms and two nitrogen atoms of the ligands L (Zn(1)-N(1), 2.036(4) ; Zn(1)-N(3), 2.043(4) ; Zn(1)-Cl(1), 2.225(2) ; Zn(1)-Cl(2), 2.220(2) ; angles NZnN, 106.1(2)A degrees; ClZnCl, 116.47(7)A degrees). The complexes are combined into a 1D supramolecular structure by nonclassical hydrogen bonds C-H center dot center dot center dot Cl and pi-pi-stacking interaction between centrosymmetric pairs of aromatic rings of one of the independent ligands. The compounds [CdI2(Phtz)] and [HgBr2(Phtz)] have also been synthesized, and their luminescent properties have been studied.

If you are interested in 737-31-5, you can contact me at any time and look forward to more communication. HPLC of Formula: https://www.ambeed.com/products/737-31-5.html.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, molecular formula is , belongs to phthalazine compound. In a document, author is Ayala, Gerardo, SDS of cas: 737-31-5.

A total of five new CuSCN-LL complexes with aromatic diimine ligands, LL = quinoxaline (Qox), quinazoline (Qnz), phthalazine (Ptz), 2-aminopyrazine (2-NH(2)Pyz), and 2-methoxypyrazine (2-MeOPyz) have been prepared and characterized by crystallographic methods. The following compounds are reported: (CuSCN)(2)(Qox) (1), (CuSCN)(Qnz) (2), (CuSCN)(2)(Ptz) (3), (CuSCN)(2)(2-NH2Pyz) (4), and (CuSCN)(2-MeOPyz) (5). Compounds 1-4 were prepared using an extended aqueous reflux method in the presence of KSCN and ammonia. Compound 5 was prepared by directly reacting solid CuSCN with the liquid ligand. In complexes 2 and 5, LL is monodentate, while in others LL is bridging bidentate. All network structures are 2-D sheets, consisting of mu(2)-LL-crosslinked CuSCN ladders for 1 and 4, LL-decorated CuSCN sheets for 2 and 5, and unusual mu(2)-LL-stapled sheets for 3. (C) 2016 Elsevier Ltd. All rights reserved.

If you are hungry for even more, make sure to check my other article about 737-31-5, SDS of cas: 737-31-5.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Electric Literature of 737-31-5, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, SMILES is O=C([O-])C1=C(I)C(NC(C)=O)=C(I)C(NC(C)=O)=C1I.[Na+], belongs to phthalazine compound. In a article, author is Jadhav, Amol Maruti, introduce new discover of the category.

An efficient, inexpensive and environmentally friendly synthesis of novel 3-amino-2-benzoyl-1-aryl-1H-pyrazolo[1,2 b]phthalazine 5,10-dione and 3-amino-2-benzoyl-1-aryl-1H-pyrazolo[1,2-a]pyridazine-5,8-dione derivatives has been developed via one-pot three-component reaction of phthalhydrazide or maleic hydrazide, aldehydes and arylacetonitrile in the presence of catalytic amount of InCl3 as a Lewis acid catalyst under solvent-free conditions. The most important features of the present protocol are mild reaction conditions, short reaction times, high yields, and a wide range of functional group tolerance. (C) 2019 Elsevier Ltd. All rights reserved.

Electric Literature of 737-31-5, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 737-31-5.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , Category: phthalazines, 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, molecular formula is C11H8I3N2NaO4, belongs to phthalazine compound. In a document, author is Maftei, Dan, introduce the new discover.

The X-ray crystal structure of 8-(4-methylbenzoyl)benzo[5,6]isoindolo[1,2-a]phthalazine-9,14-dione, a derivative of fused pyrrolophtalazine heterocycle, is reported. The compound crystallfzes in the monoclinic C2/c space group (no. 15) with a = 23.968(4) angstrom, b = 7.6709(14) angstrom, c = 22.353(3) angstrom, alpha = gamma = 90.00, beta = 110.680(15)degrees, V=3845 angstrom(3) and Z = 7. Molecular and crystal packing parameters for the novel heterocyclic system were obtained from intensity data collected at room temperature. Both the benzo [5,6]isoindolo [1,2-a]phthalazine-9,14-dione and the 4-methyl-benzoyl fragments are planar and oriented at 78 degrees. Crystal packing is based on multiple (strong) pi-pi stacking interactions.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 737-31-5. Category: phthalazines.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Reference of 737-31-5, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, SMILES is O=C([O-])C1=C(I)C(NC(C)=O)=C(I)C(NC(C)=O)=C1I.[Na+], belongs to phthalazine compound. In a article, author is Han, Young Taek, introduce new discover of the category.

In the recent decades, N-heterocycles are widely used as versatile scaffolds for the development of biologically active compounds and considered as one of the privileged structures. Among the various N-heterocycles, benzodiazines, a series of bicyclic heterocycles in which benzene rings are fused with 6-membered heterocycles containing two nitrogens are especially interesting, due to their structural conciseness and usefulness as synthetic intermediates, and suitable physicochemical properties as potential drug candidates and chemical probes. For this reason, a series of synthetic methodologies for benzodiazines has been developed and generally used in organic and medicinal chemistry fields. Interestingly, synthesis of quinazoline, a kind of benzodiazine in which benzene is fused with pyrimidine, has been extensively reviewed, while cinnoline, phthalazine and quinoxaline, benzene fused with pyridazine or pyrazine, have been relatively less investigated. In this review, recent advances in the synthesis of biologically active benzodiazines, benzene ring-fused 6-membered heterocycles with two nitrogen atoms, cinnoline, phthalazine and quinoxaline, will be addressed. In each section, biological activities of various benzodiazines, recently served as novel scaffolds for drug discovery, are briefly summarized for comprehensive understanding of biological and medicinal significance in advance. Moreover, intensive investigation of the synthetic approaches to various benzodiazines such as cinnoline, phthalazine and quinoxaline is followed. It would hopefully be helpful for the readers who have interests in developing novel drug candidates and related useful chemical probes.

Reference of 737-31-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 737-31-5.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Application of 737-31-5, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, SMILES is O=C([O-])C1=C(I)C(NC(C)=O)=C(I)C(NC(C)=O)=C1I.[Na+], belongs to phthalazine compound. In a article, author is Jiang, Lilin, introduce new discover of the category.

Cu@Fe3O4 MNPs as novel nanomagnetic reagents were prepared to investigate their catalytic behavior in the preparation of tetrahydrobenzimidazo[2,1-b]quinazolin-1(2H)-ones, as important biologically active compounds. Then, characterization of the synthesized nanoparticles was performed using different methods including Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) analysis, thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), energy dispersive X-ray (EDX), and scanning electron microscopy (SEM). All reactions were performed with small amounts of the Cu@Fe3O4 MNPs under solvent-free conditions. After completion of the reaction, because of the magnetic nature of the nanocatalyst, they could be simply separated with an external magnet and easily reused with no considerable decrease in the catalytic behavior even after seven runs.

Application of 737-31-5, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about 737-31-5 is helpful to your research.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Reference of 737-31-5, Catalysts allow a reaction to proceed via a pathway that has a lower activation energy than the uncatalyzed reaction. 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, SMILES is O=C([O-])C1=C(I)C(NC(C)=O)=C(I)C(NC(C)=O)=C1I.[Na+], belongs to phthalazine compound. In a article, author is Hosseininasab, N., introduce new discover of the category.

A novel heterogeneous acidic ionic liquid based on functionalized imidazolium salt of phosphotungstic acid (H3PW12O40, denoted as PW), immobilized on CuFe2O4@SiO2 magnetic nanoparticles, denoted as CuFe2O4@SiO2@C-3-Imid-C4SO3-PW, was prepared and characterized using FT-IR, SEM, EDX, and VSM techniques. High activity of the prepared material as a novel catalyst was evaluated in one-pot synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-diones by reaction of phthalhydrazide with an aromatic aldehyde and malononitrile under solvent-free conditions. The process gave high yields of the products over short reaction time. The catalyst was efficiently recovered by magnetic decantation and used repeatedly without significant loss of its activity.

Reference of 737-31-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 737-31-5.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. The former is the study of compounds containing at least one carbon-hydrogen bonds. 737-31-5, Name is Sodium 3,5-diacetamido-2,4,6-triiodobenzoate, molecular formula is C11H8I3N2NaO4, belongs to phthalazine compound, is a common compound. In a patnet, author is Raghavendra, G. Jeevan, once mentioned the new application about 737-31-5, Application In Synthesis of Sodium 3,5-diacetamido-2,4,6-triiodobenzoate.

One-Pot Four Component Synthesis of 3-Amino-1-(1H-indol-2-yl)-5,10-dioxo-5,10-dihydro-1H-pyrazolo[1,2-b]phthalazine Derivatives Mediated by [DBUH][OAc]

One-pot, four component, green, and efficient synthesis of 3-amino-1-(5-nitro-1H-indol-2-yl)-5,10-dioxo-5,10-dihydro-1H-pyrazolo[1,2-b]phthalazine derivatives by reaction of phthalic anhydride with hydrazine hydrate, 5-nitro-1H-indole-3-carboxaldehyde-indole-3-carboxaldehydes and malononitrile-ethyl cyanoacetate in the presence of [DBUH][OAc] at 60-65 degrees C is developed. The method is characterized by short reaction time, high yields, and purity of products formed.

We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, 737-31-5. The above is the message from the blog manager. Application In Synthesis of Sodium 3,5-diacetamido-2,4,6-triiodobenzoate.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem