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Here is just a brief introduction to this compound(19777-66-3)Name: (S)-Propane-1,2-diamine dihydrochloride, more information about the compound((S)-Propane-1,2-diamine dihydrochloride) is in the article, you can click the link below.

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, European Journal of Organic Chemistry called Unprecedented Asymmetric Epoxidation of Isolated Carbon-Carbon Double Bonds by a Chiral Fluorous Fe(III) Salen Complex: Exploiting Fluorophilic Effect for Catalyst Design, Author is Kobayashi, Yuki; Obayashi, Riho; Watanabe, Yuki; Miyazaki, Hiroki; Miyata, Issei; Suzuki, Yuta; Yoshida, Yukihiro; Shioiri, Takayuki; Matsugi, Masato, which mentions a compound: 19777-66-3, SMILESS is C[C@H](N)CN.[H]Cl.[H]Cl, Molecular C3H12Cl2N2, Name: (S)-Propane-1,2-diamine dihydrochloride.

The first asym. epoxidation of isolated carbon-carbon double bonds by a chiral salen complex using ubiquitous Fe(III) as a center-metal was described. By simultaneously introducing fluorous tags and tert-Bu groups into the ligand of the salen complex, asym. epoxidation was achieved. The fluorous tags act as both the electron-withdrawing groups, to improve the catalytic activity for oxidation, and the driving force to form a unique asym. stereo environment. Crystallog. anal. of the complex revealed that the catalyst has a distinctive umbrella structure based on intramol. fluorophilic effect. This is the first example of asym. catalytic space construction that exploits fluorous space-interaction of neighboring fluorous tags.

Here is just a brief introduction to this compound(19777-66-3)Name: (S)-Propane-1,2-diamine dihydrochloride, more information about the compound((S)-Propane-1,2-diamine dihydrochloride) is in the article, you can click the link below.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider