Chemical engineers work across a number of sectors, processes differ within each of these areas, but chemistry and chemical engineering roles are found throughout, creation and manufacturing process of chemical products and materials. Application In Synthesis of Ethyl 3-aminobenzoate methanesulfonate, 886-86-2, Name is Ethyl 3-aminobenzoate methanesulfonate, SMILES is O=C(OCC)C1=CC=CC(N)=C1.CS(=O)(O)=O, in an article , author is Thiel, Oliver R., once mentioned of 886-86-2.
The need to access different heterocyclic cores as part of p38 MAP kinase inhibitors led to the discovery and development of several efficient approaches to three separate classes of heterocycles, namely phthalazines, pyrazolopyridinones, and triazolopyridines. This account summarizes our studies in this field in a comprehensive fashion. 1 Introduction 2 Synthesis of Phthalazine-Based p38 Inhibitors 2.1 Synthesis of Clinical Candidate 2 2.2 Synthesis of Clinical Candidate 3 3 Synthesis of Pyrazolopyridinone-Based p38 Inhibitors 4 Synthesis of Triazolopyridine-Based p38 Inhibitors 4.1 Synthesis through Pd-Catalyzed Benzhydrazide Couplings 4.2 Synthesis through Pd-Catalyzed Benzhydrazone Couplings 5.0 Conclusions
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 886-86-2. Application In Synthesis of Ethyl 3-aminobenzoate methanesulfonate.
Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem