Properties and Exciting Facts About 79098-85-4

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application of 79098-85-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 79098-85-4, in my other articles.

Application of 79098-85-4, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 79098-85-4, Name is 3-(Piperidin-4-yl)indolin-2-one hydrochloride, molecular formula is C13H17ClN2O. In a Article,once mentioned of 79098-85-4

We synthesized a series of arylalkyl piperidines (II) carrying a heterocycle at the 4-position of piperidine and examined the hypotensive activities of the products. Compound 23 had the highest hypotensive activity in anesthetized normotensive rats (-78mmHg, 30 mg/kg, i.p.) and compound 12 showed the strongest hypotensive activity (-95 mmHg, 30 mg/kg, p.o.) in unanesthetized spontaneously hypertensive rats. Only compound 16 produced a considerable decrease in blood pressure in both animal models.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Application of 79098-85-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 79098-85-4, in my other articles.

Reference:
Piperidine – Wikipedia,
Piperidine | C5H20878N – PubChem

 

Brief introduction of 79098-85-4

The synthetic route of 79098-85-4 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.79098-85-4,3-(Piperidin-4-yl)indolin-2-one hydrochloride,as a common compound, the synthetic route is as follows.,79098-85-4

EXAMPLE 179 4-(2-Oxo-2,3-dihydroindol-3-yl)-1-(3-phenoxypropyl)piperidine STR215 From a mixture of 4-[2-oxo-2,3-dihydroindol-3-yl)piperidine hydrochloride (198 mg, 0.73 mmol), 3-phenoxy-propyl chloride (476 mg, 2.22 mmol) and K2 CO3 (138 mg) in toluene (15 mL) was obtained 170 mg (70%) of the title compound as a yellow oil, 1 H NMR (CDCl3): 1.42-1.50 (m, 2H), 1.79-2.03 (m, 6H), 2.10-2.15 (m, 1H), 2.47-2.52 (m, 2H), 2.90-3.04 (m, 2H), 3.408 (d, 1H, J=3.5), 7.001 (t, 1H, J=7.5), 7.022 (t, 1H, J=7.5), 7.23-7.29 (m, 3H), 7.909 (s, 1H). The hydrochloride mp 182-3 C.

The synthetic route of 79098-85-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Warner-Lambert Company; Cocensys, Incorporated; US6124323; (2000); A;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem