The Absolute Best Science Experiment for (3-Phenyl-5-isoxazolyl)methanol

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 90924-12-2

Related Products of 90924-12-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.90924-12-2, Name is (3-Phenyl-5-isoxazolyl)methanol, molecular formula is C10H9NO2. In a article,once mentioned of 90924-12-2

The invention of formula (I) indicated by the nicotinic acid derivatives and its pharmaceutically acceptable salt or solvate thereof, Wherein Z is selected from O, S, NR3 , Wherein R3 C is hydrogen or1 – 6 Alkyl; R1 Or R2 Selected independently from hydrogen, C1 – 6 Alkyl, C1 – 6 Alkoxy, halogenated C1 – 6 Alkyl, halogen, cyano, nitro, aryl, aryl oxy, heteroaryl, heteroaryl oxy, heterocyclyl, heterocyclic yloxy; said C1 – 6 Alkyl, C1 – 6 Alkoxy, halogenated C1 – 6 Alkyl, aryl, heteroaryl, heterocyclic radical may be optionally substituted pyridyl substituted, the substituents can be: C1 – 6 Alkyl, C1 – 6 Alkoxy, halogenated C1 – 6 Alkyl, halogen, cyano, nitro, aryl; m is 0 – 4 integer; n is 0 – 5 integer. The compound or its salt to colon cancer cell line HCT – 116, human lung cancer cell strain A549 and breast cancer cell MCF – 7 has very strong inhibiting activity. In addition, this kind of compound anticancer active broad-spectrum, can be used to treat the tumor, cancer and other diseases of the candidate drug or a lead compound. (by machine translation)

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 90924-12-2

Reference:
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem