Category: 50382-32-6

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.50382-32-6, Name is (2,4-Dimethylthiazol-5-yl)methanol, molecular formula is C6H9NOS. In a Patent，once mentioned of 50382-32-6, HPLC of Formula: C6H9NOS

The present invention provides a novel pyrazole derivative and an androgen receptor antagonist containing the derivative. The present invention provides a compound represented by the formula (I) wherein R1 is a hydrogen atom, a group via a carbon atom, a group via a nitrogen atom, a group via an oxygen atom, or a group via a sulfur atom; R2 is a phenyl group having cyano (the phenyl group may further have substituent(s) other than cyano); R3 is a hydrogen atom, a group via a carbon atom, a group via a nitrogen atom, a group via an oxygen atom, or a group via a sulfur atom; R4 is a cyclic group optionally having substituent(s); and X is methylene optionally having substituent(s), or CO, 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.HPLC of Formula: C6H9NOS, you can also check out more blogs about50382-32-6

Reference：
Thiazole | C3H12NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 50382-32-6. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 50382-32-6, Name is (2,4-Dimethylthiazol-5-yl)methanol

Compounds of the general formula (I): or salts thereof, which exhibit CCR5 antagonism and exert preventive and therapeutic effects against HIV infections: wherein R1 is a 5-to 6-membered aromatic ring which bears a substituent represented by the general formula: R-Z1-X-Z2-(wherein R1 is hydrogen or optionally substituted hydrocarbyl; X is optionally substituted alkylene; and Z1 and Z2 are each a heteroatom) and may be further substituted, with R being optionally bonded to the aromatic ring to form another ring; Y is optionally substituted imino; and R2 and R3 are each optionally substituted aliphatic hydrocarbyl or an optionally substituted hetero-alicyclic group.

If you are hungry for even more, make sure to check my other article about 50382-32-6. Related Products of 50382-32-6

Reference：
Thiazole | C3H19NS – PubChem,
Thiazole | chemical compound | Britannica

50382-32-6, Name is (2,4-Dimethylthiazol-5-yl)methanol, molecular formula is C6H9NOS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 50382-32-6, Safety of (2,4-Dimethylthiazol-5-yl)methanol

The disclosure generally relates to compounds of formula I, II, III and IV, including compositions and methods for treating human immunodeficiency virus (HIV) infection. The disclosure provides novel inhibitors of HIV, pharmaceutical compositions containing such compounds, and methods for using these compounds in the treatment of HIV infection.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of (2,4-Dimethylthiazol-5-yl)methanol. In my other articles, you can also check out more blogs about 50382-32-6

Reference£º
Thiazole | C3H13NS – PubChem,
Thiazole | chemical compound | Britannica