A new application about 4-(Methylthio)benzaldehyde

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 3446-89-7, in my other articles. Recommanded Product: 3446-89-7.

Chemistry is an experimental science, Recommanded Product: 3446-89-7, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 3446-89-7, Name is 4-(Methylthio)benzaldehyde, molecular formula is C8H8OS, belongs to pyrrolines compound. In a document, author is Ma, SM.

Unexpected facile sequential halolactamization-hydroxylation of 2,3-allenamides with CuX2 for the efficient synthesis of 4-halo-5-hydroxypyrrol-2(5H)-ones

[GRAPHICS] 4-Halo-5-hydroxypyrrol-2(5H)-ones were synthesized from the efficient sequential halolactamization-hydroxylation reaction of 4-monosubstituted 2,3-allenamides with CuX2 (X = Br, CI) in high yields. Halolactamization of fully substituted 2,3-dienamide (1f) afforded 4-halo-pyrrol-2(5H)-ones.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 3446-89-7, in my other articles. Recommanded Product: 3446-89-7.

Reference:
Pyrroline – Wikipedia,
,1-Pyrroline | C4H7N – PubChem