Properties and Exciting Facts About 40138-16-7

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction. 40138-16-7. The above is the message from the blog manager. Safety of (2-Formylphenyl)boronic acid.

New Advances in Chemical Research in 2021. As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. In an article, author is Li, Xin-Sheng, once mentioned the application of 40138-16-7, Name is (2-Formylphenyl)boronic acid, molecular formula is C7H7BO3. Now introduce a scientific discovery about this category, Safety of (2-Formylphenyl)boronic acid.

In the title compound, C(20)H(18)B(2)F(4)N(6), the bis(5,7-dimethyl-1,8-naphthyridin-2-yl) diazene molecule is bisected by a symmetry centre midway between the central N atoms of the diazene group. Each of the symmetry-related halves of the molecule binds to a B atom through an N,N’-bite. Two terminal F ions complete the distorted BN(2)F(2) tetrahedral geometry around each B atom. The BF(2) plane is almost perpendicular to the boron-naphthyridine ring plane, with a dihedral angle of 87.8 (2)degrees. The main interactions in the crystal structure are some C-H center dot center dot center dot F hydrogen bonds and pi-pi contacts between 1,8-naphthyridine rings [centroid-centroid distance = 4.005 (1) angstrom].

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction. 40138-16-7. The above is the message from the blog manager. Safety of (2-Formylphenyl)boronic acid.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem