More research is needed about 832720-36-2

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. you can also check out more blogs about 832720-36-2. Product Details of 832720-36-2.

Chemistry, like all the natural sciences, Product Details of 832720-36-2, begins with the direct observation of nature¡ª in this case, of matter.832720-36-2, Name is Elagolix sodium, SMILES is O=C([O-])CCCN[C@H](C1=CC=CC=C1)CN(C(N(CC2=C(C(F)(F)F)C=CC=C2F)C(C)=C3C4=CC=CC(OC)=C4F)=O)C3=O.[Na+], belongs to pyrimidines compound. In a document, author is Leyva-Acuna, Mario A., introduce the new discover.

Ethyl (S)-2-Benzamido-5-[(4,6-dimethylpyrimidin-2-yl)amino]pentanoate

Pyrimidines are compounds with a wide range of biological activities, and the synthesis of pyrimidine derivatives-useful in chemical and medicinal applications-is important in medicinal chemistry. This work shows the synthesis under microwave irradiation of the novel compound ethyl (S)-2-benzamido-5-[(4,6-dimethylpyrimidin-2-yl)amino]pentanoate (3) from (S)-N-alpha-benzoyl-l-arginine ethyl ester hydrochloride (1) and acetylacetone (2). Compound 3 was easily purified, obtained in moderate yield (70%), and fully characterized by UV-Vis, FTIR-ATR spectroscopy, H-1-NMR, C-13-NMR, HRMS, and EI-MS.

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. you can also check out more blogs about 832720-36-2. Product Details of 832720-36-2.

Reference:
Pyrimidine | C4H4N2 – PubChem,
,Pyrimidine – Wikipedia