Extended knowledge of 2,2-Dimethyl-2,3-dihydrobenzofuran-7-ol

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 1563-38-8

Electric Literature of 1563-38-8, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1563-38-8, Name is 2,2-Dimethyl-2,3-dihydrobenzofuran-7-ol, molecular formula is C10H12O2. In a Patent£¬once mentioned of 1563-38-8

2 – (Benzofuran -7 – oxy) – N’ – substituted aryl/alkyl formylcyanoacetylhydrazone derivative and its preparation method and application (by machine translation)

The present invention provides a compound of formula (I) indicated by the 2 – (benzofuran – 7 – yloxy) – N’ – substituted aryl/alkyl formylcyanoacetylhydrazone derivative and its preparation method and application, in the formula, R is selected from 4 – CN – C6 H4 , 4 – F – C6 H4 , 4 – Cl – C6 H4 , 4 – Br – C6 H4 , 3 – F – C6 H4 , 3 – Br – C6 H4 , 4 – NO2 – C6 H4 , 3 – NO2 – C6 H4 , 2 – Br – C6 H4 , 3 – CH3 – C6 H4 , 4 – CH3 – C6 H4 , 4 – OMe – C6 H4 , 3 – OMe – C6 H4 , 2 – OMe – C6 H4 , Phenyl, isopropyl, cyclohexane, styryl, furyl, thiophene base or naphthyl. The compounds of this invention and its pharmaceutically acceptable salt at a relatively low dosage, human breast cancer cells (MCF – 7), human cervical carcinoma cells (HeLa), human stomach cancer cell (MGC – 803), human lung adenocarcinoma cells (A549), human breast cancer cells (MDA – MB – 231) inhibitory activity, for the anti-tumor drug provides a new selection. (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 1563-38-8

Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H2313O – PubChem