Day: August 20, 2021

Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 162167-97-7, molcular formula is C11H22N2O2, introducing its new discovery. Formula: C11H22N2O2

The present invention provides compounds, compositions thereof, and methods of using the same.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H17086N – PubChem

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent， HPLC of Formula: C11H20BrNO2, Which mentioned a new discovery about 158407-04-6

There is provided an imidazole derivative useful as a thrombosis treating agent, which is represented by the formula (I): wherein R represents an optionally substituted cyclic hydrocarbon group or an optionally substituted heterocyclic group, W represents a bond or an optionally substituted divalent linear hydrocarbon group, X represents an optionally substituted divalent hydrocarbon group, Y represents -CO-, -S(O)-, -S(O)2- or a bond, ring A represents an optionally substituted pyrrolidine ring, an optionally substituted piperidine ring or an optionally substituted perhydroazepine ring, Z1 and Z3 independently represent a bond or an optionally substituted divalent linear hydrocarbon group, Z2 represents -N(R1)-, -O-, – S(O)-, -S(O)2-, -CO-, -CH(R1)- or a bond, ring B represents an optionally substituted imidazole ring, wherein a substituent which the optionally substituted imidazole ring represented by ring B may have may be taken together with R1 to form an optionally substituted ring, and a represents 0, 1 or 2.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H22465N – PubChem

Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 140645-23-4, molcular formula is C11H22N2O2, introducing its new discovery. Recommanded Product: 140645-23-4

The color additive, Allura Red AC, was given in the diet to provide levels of 0.42, 0.84, and 1.68% (control, 0%), from 5 weeks of age of the F0 generation to 9 weeks of age of the F1 generation in mice, and selected reproductive and neurobehavioral parameters were measured. There were few adverse effects of Allura Red AC on either litter size or weight, and ratio of male to female was significantly reduced in the lowest dosed group. Average body weight of offspring during the lactation period was significantly increased in the lower dosed groups of each sex. As regards the neurobehavioral parameters, no adverse effect was observed in the behavioral development during lactation period. There were few adverse effects of Allura Red AC on either movement activity or maze learning in F1 generation mice, compared with controls in each sex. The dose levels of Allura Red AC in the present study (approximately 86-1430 times greater than human ADI) produced few adverse effects in reproductive and neurobehavioral parameters in mice.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H16685N – PubChem

Synthetic Route of 68947-43-3, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.68947-43-3, Name is 1-Methylpiperidine-4-carboxylic acid, molecular formula is C7H13NO2. In a Patent，once mentioned of 68947-43-3

Isoquinoline compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an isoquinoline compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer’s disease, lung disease, inflammation, auto-immune diseases and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as neurological conditions/disorders/diseases linked to overexpression of DYRK1A.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H6950N – PubChem

Electric Literature of 142247-38-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 142247-38-9, Name is 4-(1-(tert-Butoxycarbonyl)piperidin-4-yl)butanoic acid, molecular formula is C14H25NO4. In a Article，once mentioned of 142247-38-9

A survey of charged groups and linkers for a series of symmetrical and unsymmetrical dibasic inhibitors is described, leading to several classes of potent and selective inhibitors. In particular, the benzamidine functionality was identified as the most potent charged group investigated.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H21875N – PubChem

Chemistry is traditionally divided into organic and inorganic chemistry. Recommanded Product: 2213-43-6. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 2213-43-6

The present invention relates to compounds of formula I and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prophylaxis of diseases which are associated with the modulation of CB1 receptors.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H725N – PubChem

Reference of 26371-07-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.26371-07-3, Name is 3-(Piperidin-1-yl)propanoic acid, molecular formula is C8H15NO2. In a article，once mentioned of 26371-07-3

After solvent evaporation 1 – (3 – (3 – (4 – of) chlorophenyl) propyl) piperidine – 1 1-yl, propionic acid solution :S1, is added into the reactor 3 – (4 – to react)-chlorophenyl-3 – (-propyl-)-propan ;S2,yl, propionic acid solution 3 – (4 – to)-chlorophenyl-3 – (-propynyl) piperi- 1 1-yl, propionate solution . The method comprises the following steps 3 – (4 – preparing)-chlorophenoxy-3 – (-propan) piperi- 1 1-yl) ;S3, propionate in a reactor at a certain temperature 3 – (4 – and) adding a solid super strong acid) to obtain ;S4, the target product 3 – (-), phenyl)-propoxy-propyl 3 – (4 -) piperidinetanyl hydrochloride. 3 – (4 -)). 3 – (The. invention is low in cost 1 – (3 – (3 – (4 – 3 – (yield))-yl propionate 50-70 C, toluene 4-8 solution by adding a solid super-strong acid. (by machine translation)

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H9182N – PubChem

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Computed Properties of C10H20N2O2, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 73874-95-0, Name is tert-Butyl piperidin-4-ylcarbamate, molecular formula is C10H20N2O2. In a Article, authors is Kathiravan, Subban，once mentioned of 73874-95-0

Metal-catalyzed cross-coupling reactions are among the most important transformations in organic synthesis. However, the use of C-H activation for sp2 C-N bond formation remains one of the major challenges in the field of cross-coupling chemistry. Described herein is the first example of the synergistic combination of copper catalysis and electrocatalysis for aryl C-H amination under mild reaction conditions in an atom-and step-economical manner with the liberation of H2 as the sole and benign byproduct.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H14160N – PubChem

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent， SDS of cas: 50541-93-0, Which mentioned a new discovery about 50541-93-0

The present invention relates to a novel method for synthesizing imidazole derivatives having 4-aryl, 5-pyrimidine heterocyclic rings using a novel cycloaddition reaction.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H12276N – PubChem

Electric Literature of 6574-15-8, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 6574-15-8, Name is 1-(4-Nitrophenyl)piperidine, molecular formula is C11H14N2O2. In a Article，once mentioned of 6574-15-8

Magnetic graphitic carbon nitride, Fe@g-C3N4, has been synthesized by adorning a graphitic carbon nitride (g-C3N4) support with iron oxide via non-covalent interaction. The magnetically recyclable catalyst showed excellent reactivity for the expeditious C-H activation and cyanation of amines.

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Reference：
Piperidine – Wikipedia,
Piperidine | C5H15320N – PubChem