Electric Literature of 254-60-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.254-60-4, Name is 1,8-Diazanaphthalene, molecular formula is C8H6N2. In a Article£¬once mentioned of 254-60-4
The syntheses and crystal structures of N-(7-bromomethyl-1, 8-naphthyridin-2- yl)acetamide dioxane hemisolvate, C11H10BrN3?0.5C4H8O2, (I), and bis[N-(7- dibromomethyl-1, 8-naphthyridin-2-yl)acetamide] dioxane hemisolvate, 2C11H9Br2N3?0.5C4H8O2, (II), are described. The molecules adopt a conformation with the N-H hydrogen pointing towards the lone electron pair of the adjacent naphthyridine N atom. The crystals of (I) are stabilized by a three-dimensional supramolecular network comprising N-H?N, C-H?N and C-H?O hydrogen bonds, as well as C-Br?pi halogen bonds. The crystals of compound (II) are stabilized by a three-dimensional supramolecular network comprising N-H?N, C-H?N and C-H?O hydrogen bonds, as well as C-H?pi contacts and C-Br?pi halogen bonds. The structure of the substituent attached in the 7-position of the naphthyridine skeleton has a fundamental influence on the pattern of intermolecular noncovalent bonding. While the Br atom of (I) participates in weak C-Br?Oguest and C-Br?picontacts, the Br atoms of compound (II) are involved in host-host interactions via C-Br?O C, C-Br?N and C-Br?pi bonding.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 254-60-4
Reference£º
1,243-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N237 – PubChem