Category: 179474-79-4

Synthetic Route of 179474-79-4, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 179474-79-4, Name is 1-(3-Methoxypropyl)piperidin-4-amine, molecular formula is C9H20N2O. In a Patent£¬once mentioned of 179474-79-4

A process for the preparation of intermediate the Pu card must benefit new process (by machine translation)

The invention discloses a compound of formula (I) indicated by the 1 – (3 – a oxygen propyl) – 4 – amino piperdine preparation method, it includes such as the following steps: (1) a compound of formula (II) in the reaction in a solution of ammonia the system results in the type (III) compound; (2) the compound of formula (III) with 1, 3 – dibromo – 5, 5 – dimethyl hydantoin in the reaction under alkaline condition is the system results in the type (I) compound. This preparation method without special reaction equipment requirements, the operation is simple, and is suitable for industrial production; high yield, three wastes, low cost; high purity, heavy metal residue problem. (by machine translation)

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Synthetic Route of 179474-79-4, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 179474-79-4, in my other articles.

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H10411N – PubChem

 

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬ category: piperidines, Which mentioned a new discovery about 179474-79-4

Biochemical and biophysical characterization of unique switch pocket inhibitors of p38alpha

Herein we describe the identification and characterization of a class of molecules that are believed to extend into a region of p38 known as the ‘switch pocket’. Although these molecules lack a canonical hinge binding motif, they show Ki values as low as 100 nM against p38. We show that molecules that interact with this region of the protein demonstrate different binding kinetics than a canonical ATP mimetic, as well as a wide range of kinome profiles. Thus, the switch pocket presents new opportunities for kinome selectivity which could result in unique biochemical responses and offer new opportunities in the field of kinase drug discovery.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 179474-79-4, help many people in the next few years.category: piperidines

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H10413N – 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, 179474-79-4, molcular formula is C9H20N2O, introducing its new discovery. Quality Control of: 1-(3-Methoxypropyl)piperidin-4-amine

A process for preparing 1 – (3 – a oxygen propyl) piperidine – 4 – amine (by machine translation)

The invention discloses a method for preparing 1-(3-methoxypropyl)-4-piperidinamine. The method includes the following steps: the raw material, namely 4-aminopiperdine is adopted, primary amine is selectively protected by benzophenone based on the difference of chemical properties of primary amine and secondary amine, free secondary amine is subjected to proton abstraction, then the free secondary amine subjected to proton abstraction reacts with 3-methoxy-bromopropane, under the acid condition, the protecting group is removed, and finally, the product is obtained. The synthetic process is simple to operate, besides, the removed protecting group subjected to simple treatment can be recycled, and industrial enlarged production is facilitated.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Quality Control of: 1-(3-Methoxypropyl)piperidin-4-amine, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 179474-79-4

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H10410N – PubChem