Category: 131748-97-5

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.131748-97-5, Name is (2-(Trifluoromethyl)thiazol-5-yl)methanol, molecular formula is C5H4F3NOS. In a Patent，once mentioned of 131748-97-5, Formula: C5H4F3NOS

An insecticidal composition containing a guanidine derivative of the formula: STR1 wherein R1 is an optionally substituted homocyclic or heterocyclic group, n is 0 or 1, R2 is a hydrogen atom or an optionally substituted hydrocarbon group, R3 is a primary, secondary or tertiary amino group, X is an electron attractive group such as nitro or trifluoroacetyl group, provided that when n is 0, R1 is an optionally substituted heterocyclic group or a salt thereof.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Formula: C5H4F3NOS, you can also check out more blogs about131748-97-5

Reference：
Thiazole | C3H5NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 131748-97-5, Chemistry can be defined as the study of matter and the changes it undergoes. You’ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.131748-97-5, Name is (2-(Trifluoromethyl)thiazol-5-yl)methanol, molecular formula is C5H4F3NOS. In a patent, introducing its new discovery.

We report herein the design and synthesis of a series of orally active, liver-targeted hypoxia-inducible factor prolyl hydroxylase (HIF-PHD) inhibitors for the treatment of anemia. In order to mitigate the concerns for potential systemic side effects, we pursued liver-targeted HIF-PHD inhibitors relying on uptake via organic anion transporting polypeptides (OATPs). Starting from a systemic HIF-PHD inhibitor (1), medicinal chemistry efforts directed toward reducing permeability and, at the same time, maintaining oral absorption led to the synthesis of an array of structurally diverse hydroxypyridone analogues. Compound 28a was chosen for further profiling, because of its excellent in vitro profile and liver selectivity. This compound significantly increased hemoglobin levels in rats, following chronic QD oral administration, and displayed selectivity over systemic effects.

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Reference：
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 131748-97-5, Name is (2-(Trifluoromethyl)thiazol-5-yl)methanol,molecular formula is C5H4F3NOS, is a conventional compound. this article was the specific content is as follows.Quality Control of: (2-(Trifluoromethyl)thiazol-5-yl)methanol

The present disclosure provides, in part, compounds having allosteric effector properties against Hepatitis B virus Cp. Also provided herein are methods of treating viral infections, such as hepatitis B, comprising administering to a patient in need thereof a disclosed compound of formula:

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Reference£º
Thiazole | C3H4NS – PubChem,
Thiazole | chemical compound | Britannica