Chemistry is an experimental science, Quality Control of: (1H-Indol-3-yl)-1-propanamine, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 6245-89-2, Name is (1H-Indol-3-yl)-1-propanamine
Glycosylation of 1,2-Dihydro-5-(1H-indol-2-yl)-1,2,4-triazole-3-thione with 2,3,4,6-tetra-O-acetyl-a-Dglucopyranosyl bromide, 2,3,4,6-tetra-O-acetyl-a-D-galactopyranosyl bromide and 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranosyl chloride was investigated in the presence of Et3N and K2CO3 as acid scavengers. A regioselective S-glycosides were obtained by using Et3N whereas, using K2CO3 gave a mixtures of two hybrids having two glycosidic bonds. The two products of each mixture were separated and characterized as S,N1-and S,N2-bis(glycosylated) derivatives. The structures of the newly synthesized compounds were elucidated by 1H NMR, 13C NMR, 2D NMR and mass spectra. The compounds were screened for their antibacterial and antifungal activities. Some compounds exhibited strong inhibition activity compared with the reference drugs (chloramphenicol and baneocin).
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Quality Control of: (1H-Indol-3-yl)-1-propanamine, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 6245-89-2, in my other articles.
Reference：
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles