Category: 7306-67-4

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. 7306-67-4, Name is 9-(Tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine, molecular formula is C10H13N5O. In a Article，once mentioned of 7306-67-4, Computed Properties of C10H13N5O

In the nematode model organisms Caenorhabditis elegans and Pristionchus pacificus, a new class of natural products based on modular assembly of primary-metabolism-derived building blocks control organismal development and behavior. We report identification and biological activities of the first pentamodular metabolite, pasa#9, and the 8-oxoadenine-containing npar#3 from P. pacificus. These structures suggest co-option of nucleoside and tryptophan metabolic pathways for the biosynthesis of endogenous metabolite libraries that transcend the dichotomy between primary and secondary metabolism.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.Computed Properties of C10H13N5O, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 7306-67-4, in my other articles.

Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics

7306-67-4, Name is 9-(Tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine, molecular formula is C10H13N5O, belongs to tetrahydropyran compound, is a common compound. In a patnet, once mentioned the new application about 7306-67-4, Recommanded Product: 9-(Tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine

Uracil derivatives form strong complexes with complementary 2,4-diaminotriazine and adenine compounds, whereas derivatives of 5-azauracil (2,4-dioxotriazine) are known to form weak complexes in aqueous medium. However, herein we report that in organic medium (CDCl3), the 5-azauracil moiety forms hydrogen-bond-mediated complexes with complementary 2,4-diaminotriazine and adenine compounds, with strengths comparable to those formed by uracil compounds. Such dichotomous base-pairing behavior of the 5-azauracil moiety, in organic versus aqueous media, is found to be consistent with the ionization of the 5-azauracil moiety in aqueous medium leading to competitive interference from water molecules (via solvation), which is absent (lack of such ionization and solvent interference) in organic medium. This discriminating role of solvent (e.g., water) could have been an important factor in the selection of molecules, based on their physicochemical properties, and subsequently in the emergence of potential primordial informational oligomers that would have played a role in the origins of life.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 9-(Tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine. In my other articles, you can also check out more blogs about 7306-67-4

Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics