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Mimi is a five-element aromatic ring compound containing two interstitary nitrogen atoms in the molecular structure, the unshared electron pair of 1-bit nitrogen atoms in the miaozole ring participates in ring conjugate, and the electron density of nitrogen atoms decreases, making the hydrogen on the nitrogen atom easily leave in the form of hydrogen ions. Therefore, Mimi is weakly acidic and can form salts with strong alkalis. The unsynchronized electron pairs of 3-bit nitrogen atoms in the mitrye ring do not participate in conjugates, but occupy sp2 hybridization orbits, which can accept protons and form salts with strong acids. The alkaline nature of mimi is slightly stronger than that of pyridine and radon. There is a phenomenon of mutual variation in the ring. Hydrogen on a 1-bit nitrogen atom can be transferred to a 3-bit nitrogen atom, so the Miele derivative, which has the same substitution base at 4-bit and 5-bit, is an intervariate construct. Mimi is stable to acid and antioxidant. Derivatives of miele are widely found in nature. Such as histamines, histamines, benzodiazepines, etc. There are some interesting reagents in the acetyl-based compounds of Mimi. For example, 1-acetylamide is a stable acetylene agent. Reacts with pyridoxine to produce 1-acetylene. In general, 1-acetylkiminazole can produce ketones and aldehydes using Gest reagents and reducing agents. N, N'-cyclobiazole reacts with niobium-based to produce a useful reagent, larynthe. The relationship between mies and natural compounds is extremely close. For example, after shrinking with the cyclospheric ring, a radon derivative is obtained, which is present in the organism in uric acid, coffee base and tea base in addition to being a base for nucleic acids such as 6-aminoquine and ostrich. The catalytic effects of methromycin, such as hydrolysis of accelerated enzymes, are being studied. Allergies to the skin are similar to binary amines. Rats pass through the mouth LD501880mg/kg.