Archives for Chemistry Experiments of 3080-99-7

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.Application In Synthesis of 3,4-Dihydro-2H-benzo[b][1,4]thiazine, you can also check out more blogs aboutApplication In Synthesis of 3,4-Dihydro-2H-benzo[b][1,4]thiazine

Chemistry, like all the natural sciences, begins with the direct observation of nature¡ª in this case, of matter. £¬Which mentioned a new discovery about 3080-99-7. Application In Synthesis of 3,4-Dihydro-2H-benzo[b][1,4]thiazine, In a article, mentioned the application of 3080-99-7, Name is 3,4-Dihydro-2H-benzo[b][1,4]thiazine, molecular formula is C8H9NS

Nitrogen-containing fused ring compounds and use thereof

A URAT1 activity inhibitor containing a nitrogen-containing fused ring compound represented by the following formula [1]: [image] wherein each symbol is as defined in the description. The present invention is useful for the prophylaxis or treatment of pathology showing involvement of uric acid, such as hyperuricemia, gouty tophus, acute gouty arthritis, chronic gouty arthritis, gouty kidney, urolithiasis, renal function disorder, coronary artery disease, ischemic heart disease and the like.

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.Application In Synthesis of 3,4-Dihydro-2H-benzo[b][1,4]thiazine, you can also check out more blogs aboutApplication In Synthesis of 3,4-Dihydro-2H-benzo[b][1,4]thiazine

Reference£º
Thiazine – an overview | ScienceDirect Topics,
Thiazine | C4H5NS – PubChem