Category: 1317-39-1

Related Products of 1317-39-1, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 1317-39-1, Copper(I) oxide, introducing its new discovery.

Benzothiophene compounds, intermediates, compositions, and method for inhibiting restenosis

The present invention provides pharmaceutically active compounds of formula I STR1 wherein R1 is –H, –OH, –O(C1 -C4 alkyl), –OCOC6 H5, –OCO(C1 -C6 alkyl), or –OSO2 (C2 -C6 alkyl); R2 is –H, –OH, –O(C1 -C4 alkyl), –OCOC6 H5, –OCO(C1 -C6 alkyl), –OSO2 (C2 -C6 alkyl), or halo, providing when Z is –S–, R2 is not halo; R3 is 1-piperidinyl, 1-pyrrolidinyl, methyl-1-pyrrolidinyl, dimethyl-1-pyrrolidinyl, 4-morpholino, dimethylamino, diethylamino, diisopropylamino, or 1-hexamethyleneimino; n is 2 or 3; and z is –O– or –S–; or a pharmaceutically acceptable salt thereof, for inhibiting restenosis.

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Reference：
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn¡¯t involve a screen. Copper(I) oxide,introducing its new discovery. Application In Synthesis of Copper(I) oxide

Phenylthioheterocyclic derivatives

Compounds of the formula STR1 wherein n is a integer of 0 to 2; R1 ‘ and R2 ‘ are, independently, hydrogen, halogen, trifluoromethyl, lower alkoxy or lower alkyl; and X is pyrimidinyl, thiazolyl or STR2 wherein R is hydrogen, lower alkyl, aryl or ar-lower alkyl; provided that at least one or R1 ‘ and R2 ‘ is other than hydrogen, and their pharmaceutically acceptable acid addition salts, and an anti-inflammatory method utilizing a compound of the formula STR3 wherein n is an integer of 0 to 2; R1 and R2 are, independently, hydrogen, halogen, trifluoromethyl, nitro, amino, lower alkylamino, di-lower-alkylamino, lower alkoxy or lower alkyl; and X is pyrimidinyl, thiazolyl or STR4 wherein R is hydrogen, lower alkyl, aryl or ar-lower alkyl; and their pharmaceutically acceptable acid addition salts, are described.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! Read on for other articles about Quality Control of (R)-4-Benzyl-2-oxazolidinone!, Application In Synthesis of Copper(I) oxide

Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

1317-39-1, Name is Copper(I) oxide, belongs to copper-catalyst compound, is a common compound. HPLC of Formula: Cu2OIn an article, once mentioned the new application about 1317-39-1.

Method of use of, and compositions containing, disubstituted xanthone carboxylic acid compounds

Compositions containing and methods employing, as the essential ingredient, novel disubstituted xanthone carboxylic acid compounds which are useful in the treatment of allergic conditions. Methods for preparing these compounds and compositions and intermediates therein are also disclosed. 5-Methylthio-7-isopropoxyxanthone-2-carboxylic acid and 5,7-di-(methylthio)xanthone-2-carboxylic acid are illustrated as representative compounds.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.HPLC of Formula: Cu2O, you can also check out more blogs aboutHPLC of Formula: Cu2O

Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Electric Literature of 1317-39-1, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 1317-39-1, Copper(I) oxide, introducing its new discovery.

Benzothiophene compounds, intermediates, compositions, and methods

The present invention provides intermediate compounds and processes for the preparation of compounds of formula I STR1 wherein R1a is –H or –OR7a in which R7a is –H or a hydroxy protecting group; R2a is –H, halo, or –OR8a in which R8a is –H or a hydroxy protecting group; R3 is 1-piperidinyl, 1-pyrrolidino, methyl-1-pyrrolidinyl, dimethyl-1-pyrrolidino, 4-morpholino, dimethylamino, diethylamino, diisopropylamino, or 1-hexamethyleneimino; n is 2 or 3; and Z is –O– or –S–; or a pharmaceutically acceptable salt thereof.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. HPLC of Formula: Cu2O. Introducing a new discovery about 1317-39-1, Name is Copper(I) oxide

Certain 6-substituted-2-pyridinamines

Certain novel substituted imidazo [1,2-a] pyridines with a substituted amino group at the 2- or 3-position are active anthelmintic agents. The novel compounds are prepared from the appropriate substituted 2-aminopyridine precursor. Compositions which utilize said novel imidazo [1,2-a] pyridines as the active ingredient thereof for the treatment of helminthiasis are also disclosed.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. HPLC of Formula: Cu2O. Introducing a new discovery about 1317-39-1, Name is Copper(I) oxide

N2O decomposition over CuO/CeO2catalyst: New insights into reaction mechanism and inhibiting action of H2O and NO by operando techniques

In this work, a combination of ex situ (STEM-EELS, STEM-EDX, H2-TPR and XPS), in situ (CO-DRIFTS) and operando (DR UV-vis and DRIFTS) approaches was used to probe the active sites and determine the mechanism of N2O decomposition over highly active 4 wt.% Cu/CeO2catalyst. In addition, reaction pathways of catalyst deactivation in the presence of NO and H2O were identified. The results of operando DR UV-vis spectroscopic tests suggest that [Cu-O-Cu]2+sites play a crucial role in catalytic N2O decomposition pathway. Due to exposure of {1 0 0} and {1 1 0} high-energy surface planes, nanorod-shaped CeO2support simultaneously exhibits enhancement of CuO/CeO2redox properties through the presence of Ce3+/Ce4+redox pair. Its dominant role of binuclear Cu+site regeneration through the recombination and desorption of molecular oxygen is accompanied by its minor active participation in direct N2O decomposition. NO and H2O have completely different inhibiting action on the N2O decomposition reaction. Water molecules strongly and dissociatively bind to oxygen vacancy sites of CeO2and block further oxygen transfer as well as regeneration of catalyst active sites. On the other hand, the effect of NO is expressed through competitive oxidation to NO2, which consumes labile oxygen from CeO2and decelerates [Cu+Cu+] active site regeneration.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Reference of 1317-39-1, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Patent, and a compound is mentioned, 1317-39-1, Copper(I) oxide, introducing its new discovery.

Tubulin binding agents and corresponding prodrug constructs

A diverse set of tubulin binding agents have been discovered which are structurally characterized, in a general sense, by a semi-rigid molecular framework capable of maintaining aryl-aryl, pseudo pi stacking distances appropriate for molecular recognition of tubulin. In phenolic or amino form, these ligands may be further functionalized to prepare phosphate esters, phosphate salts, phosphoramidates, and other prodrugs capable of demonstrating selective targeting and destruction of tumor cell vasculature.

But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! Read on for other articles about Reference of 189035-22-1!, Reference of 1317-39-1

Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

1317-39-1, Name is Copper(I) oxide, belongs to copper-catalyst compound, is a common compound. Computed Properties of Cu2OIn an article, once mentioned the new application about 1317-39-1.

alpha-Chlorocarboxylic acids

alpha-CHLOROCARBOXYLIC ACIDS OF THE FORMULA STR1 wherein Y stands for a lower alkyl group having 1 to 6 carbon atoms or a phenyl group, a benzoyl group or a phenylalkyl group having 7 to 11 carbon atoms, which may have a lower alkyl group having 1 to 3 carbon atoms, a lower alkoxy group having 1 to 3 carbon atoms or a halogen on the phenyl rings as a substituent; R1 stands for a lower alkylene group having 1 to 4 carbon atoms or a valency bond; L stands for a lower alkyl group having 1 to 3 carbon atoms; and Z stands for a carboxyl group or a group convertible to carboxyl group, are useful as, for example, remedies for hyperlipemia, diabetes and so on of mammals including human beings.

We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 1317-39-1, and how the biochemistry of the body works.Computed Properties of Cu2O

Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Application of 1317-39-1, One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, such as the rate of change in the concentration of reactants or products with time.Mentioned the application of 1317-39-1.

Photoelectrochemistry of electrodeposited Cu2O

The photoelectrochemical properties of electrodeposited Cu2O in aqueous solutions were investigated. The material showed long term stability under illumination at negative potentials. The diffusion length of electrons in the as-deposited material was of the order of 10-100 nm. We did not observe photocathodic reduction of water. The efficiencies for the reduction of oxygen and the methylviologen cation at these electrodes were surprisingly high. This suggests that, in conjunction with a suitable redox system, electrodeposited Cu2O could be a promising material as a p-type photoelectrode in an electrochemical photovoltaic cell.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. HPLC of Formula: Cu2O. Introducing a new discovery about 1317-39-1, Name is Copper(I) oxide

Substituted fused heterocyclic compound

Substituted fused heterocyclic compounds of the formula (I) and pharmacologically acceptable salts thereof: STR1wherein R 1 is a group of the formula (II) or (III): STR2R 4 is a substituted phenyl or a pyridyl which may have a substituent. R 5 is hydrogen or the like. R 6 is hydrogen, a C 1-6 alkyl group or the like. D is oxygen or sulfur. E is a CH group or nitrogen. R 2 is hydrogen or the like. R 3 is a 2,4-dioxothiazolidin-5-ylmethyl group or the like. A is a C 1-6 alkylene group. B is oxygen or sulfur. These compounds and salts are useful as the active ingredient of pharmaceutical compositions which can be used to treat patients because these compounds and salts have excellent insulin-resistance improving action, lipid-peroxide-production inhibitory action, 5-lipoxygenase inhibitory action and the like.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”