Category: 103639-57-2

Lavey, C. Flader et al. published their research in Journal of Labelled Compounds and Radiopharmaceuticals in 2011 | CAS: 103639-57-2

(S)-2-(Piperidin-2-yl)ethanol (cas: 103639-57-2) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Several piperidine alkaloids isolated from natural herbs, were found to exhibit antiproliferation and antimetastatic effects on various types of cancers both in vitro and in vivo for example Piperine, Evodiamine, Matrine, Berberine and Tetrandine.Category: piperidines

Synthesis of 3H-, 13C3-, and 14C-labeled Sch 727965 was written by Lavey, C. Flader;Hesk, D.;Koharski, D.;Truong, V.;McNamara, P.. And the article was included in Journal of Labelled Compounds and Radiopharmaceuticals in 2011.Category: piperidines This article mentions the following:

The preparation of [3H]Sch 727965 ([3H]I) from unlabeled compound and tritiated water was base catalyzed. Di-Et [13C3]malonate was used to prepare [13C3]Sch 727965 in five steps in 21.8% overall yield. In a similar manner, [14C]Sch 727965 was prepared in five steps from di-Et [2-14C]malonate in 11.1% radiochem. yield. Copyright 漏 2010 John Wiley & Sons, Ltd. In the experiment, the researchers used many compounds, for example, (S)-2-(Piperidin-2-yl)ethanol (cas: 103639-57-2Category: piperidines).

(S)-2-(Piperidin-2-yl)ethanol (cas: 103639-57-2) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Several piperidine alkaloids isolated from natural herbs, were found to exhibit antiproliferation and antimetastatic effects on various types of cancers both in vitro and in vivo for example Piperine, Evodiamine, Matrine, Berberine and Tetrandine.Category: piperidines

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

 

Lavey, C. Flader et al. published their research in Journal of Labelled Compounds and Radiopharmaceuticals in 2011 | CAS: 103639-57-2

(S)-2-(Piperidin-2-yl)ethanol (cas: 103639-57-2) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Several piperidine alkaloids isolated from natural herbs, were found to exhibit antiproliferation and antimetastatic effects on various types of cancers both in vitro and in vivo for example Piperine, Evodiamine, Matrine, Berberine and Tetrandine.Category: piperidines

Synthesis of 3H-, 13C3-, and 14C-labeled Sch 727965 was written by Lavey, C. Flader;Hesk, D.;Koharski, D.;Truong, V.;McNamara, P.. And the article was included in Journal of Labelled Compounds and Radiopharmaceuticals in 2011.Category: piperidines This article mentions the following:

The preparation of [3H]Sch 727965 ([3H]I) from unlabeled compound and tritiated water was base catalyzed. Di-Et [13C3]malonate was used to prepare [13C3]Sch 727965 in five steps in 21.8% overall yield. In a similar manner, [14C]Sch 727965 was prepared in five steps from di-Et [2-14C]malonate in 11.1% radiochem. yield. Copyright © 2010 John Wiley & Sons, Ltd. In the experiment, the researchers used many compounds, for example, (S)-2-(Piperidin-2-yl)ethanol (cas: 103639-57-2Category: piperidines).

(S)-2-(Piperidin-2-yl)ethanol (cas: 103639-57-2) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Several piperidine alkaloids isolated from natural herbs, were found to exhibit antiproliferation and antimetastatic effects on various types of cancers both in vitro and in vivo for example Piperine, Evodiamine, Matrine, Berberine and Tetrandine.Category: piperidines

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem

 

The important role of (S)-2-(Piperidin-2-yl)ethanol

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 103639-57-2

Application of 103639-57-2, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.103639-57-2, Name is (S)-2-(Piperidin-2-yl)ethanol, molecular formula is C7H15NO. In a Patent，once mentioned of 103639-57-2

A serine protease inhibitor having the formula (I), in which J is H, R1, R1?O?C(O)?, R1?C(O?, R1?SO2?, R3OOC?(CHR2)p?, (R2a,R2b)N?CO?(CHR2)p? or Het-CO?(CHR2)p?; W is an amino-acid of the formula ?NH?CHR1?C(O)?, ?NR4?CH((CH2)qC(O)OR1)?C(O)?, ?NR4?CH((CH2)qC(O)N(R2a,R2b))?C(O)?, ?NR4?CH((CH2)qC(O)Het)-C(O)?, D-1-Tiq, D-3-Tiq, D-Atc, Aic, D-1-Piq, D-3 Piq, glutanyl or a (C1-C6) alkylester thereof; E is ?NR2?CH2? or the fragment ?which is unsubstituted or substituted with (1-6C)alkyl, (1-6C)alkoxy or benzyloxy; R1 is selected form (1-12C)alkyl, (2-12C)alkenyl, (2-12C)alkynyl, (3-12C)cycloalkyl and (3-12C)cycloalkyl(1-6C)alkylene, which groups are unsubstituted or substituted with (3-12C)cycloalkyl, (1-6C)alkoxy, oxo, OH, CF3 or halogen, and from (6-14C)aryl, (7-15C)aralkyl, (8-16C)aralkenyl and (14-20C)(bisary)alkyl, wherein the aryl groups are unsubstituted or substituted with (1-6C)alkyl, (3-12C)cycloalkyl, (1-6C)alkoxy, OH, CF3 or halogen; R2, R2a and R2b are each independently selected from H, (1-C)alkyl, (3-8C)alkenyl, (3-8C)alkynyl, (3-8C)cycloalkyl and (3-6C)cycloalkyl(1-4C)alkylene, which are unsubstituted or substituted with (3-6C)cycloalkyl, (1-6C)alkoxy, CF3 or halogen, and from (6-14C)aryl and (7-15C)aralkyl, wherein the aryl groups are unsubstituted or substituted with (1-6C)alkyl, (3-6C)cycloalkyl, (1-6C)alkoxy, CF3 or halogen; R3 is the same as R2 or is Het-(1-6C)alkyl; R4 is H or (1-3C)alkyl; X and Y are CH or N, with the proviso that they are not both N; Het is a 4-, 5- or 6-membered heterocycle containing one or more heteroatoms selected from O, N and S; m is 1 or 2; p is 1, 2 or 3; q is 1, 2 or 3; t is 2, 3 or 4; or a pharmaceutically acceptable addition salt or solvate thereof.

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 103639-57-2

Reference：
Piperidine – Wikipedia,
Piperidine | C5H5118N – PubChem

 

Awesome and Easy Science Experiments about (S)-2-(Piperidin-2-yl)ethanol

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 103639-57-2 is helpful to your research. COA of Formula: C7H15NO

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 103639-57-2, name is (S)-2-(Piperidin-2-yl)ethanol, introducing its new discovery. COA of Formula: C7H15NO

Inhibition of cyclin-dependent kinases (CDKs) has emerged as an attractive strategy for the development of novel oncology therapeutics. Herein is described the utilization of an in vivo screening approach with integrated efficacy and tolerability parameters to identify candidate CDK inhibitors with a suitable balance of activity and tolerability. This approach has resulted in the identification of SCH 727965, a potent and selective CDK inhibitor that is currently undergoing clinical evaluation.

The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 103639-57-2 is helpful to your research. COA of Formula: C7H15NO

Reference：
Piperidine – Wikipedia,
Piperidine | C5H5115N – PubChem