Antiseptic imidazoles and ketones and nitrofurans

Application Reactant for: Eschenmoser coupling reaction Preparation of &#946-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions Preparation of thienylpyrazole-based thiazoles and pyrazolines as

· Eschenmoser coupling reaction · Preparation of β-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions · Preparation of thienylpyrazole-based thiazoles and pyrazolines as antimicrobial, antioxidant,

· Eschenmoser coupling reaction · Preparation of β-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions · Preparation of thienylpyrazole-based thiazoles and pyrazolines as antimicrobial, antioxidant,

· Eschenmoser coupling reaction · Preparation of β-oxo sulfones as substrates for stereoselective Michael addition/cross-benzoin cascade reactions · Preparation of thienylpyrazole-based thiazoles and pyrazolines as antimicrobial, antioxidant,

2-(N-Ethylanilino) ethanol couples with 2-amino-5-formylthiophene during the synthesis of nonlinear optical chromophores. It undergoes azo coupling with 2-cyan-4-nitroaniline to yield azochromophore AZ1Usually used in the preparation of azo compound

2-(N-Ethylanilino) ethanol couples with 2-amino-5-formylthiophene during the synthesis of nonlinear optical chromophores. It undergoes azo coupling with 2-cyan-4-nitroaniline to yield azochromophore AZ1Usually used in the preparation of azo compound

2-(N-Ethylanilino) ethanol couples with 2-amino-5-formylthiophene during the synthesis of nonlinear optical chromophores. It undergoes azo coupling with 2-cyan-4-nitroaniline to yield azochromophore AZ1Usually used in the preparation of azo compound

2-Bromo-1-methyl-1H-imidazole can be used in the synthesis of the following: · N-(4-methoxyphenyl)-1-methyl-1H-imidazol-2-amine via C-N coupling with p-anisidine · 1,2-bis[2-methyl-5-(1-methyl-1H-imidazol-2-yl)-3-thienyl]-cyclopentene, a ligand

2-Bromo-1-methyl-1H-imidazole can be used in the synthesis of the following: · N-(4-methoxyphenyl)-1-methyl-1H-imidazol-2-amine via C-N coupling with p-anisidine · 1,2-bis[2-methyl-5-(1-methyl-1H-imidazol-2-yl)-3-thienyl]-cyclopentene, a ligand

2-Bromo-1-methyl-1H-imidazole can be used in the synthesis of the following: · N-(4-methoxyphenyl)-1-methyl-1H-imidazol-2-amine via C-N coupling with p-anisidine · 1,2-bis[2-methyl-5-(1-methyl-1H-imidazol-2-yl)-3-thienyl]-cyclopentene, a ligand

2-Bromo-1-methyl-1H-imidazole can be used in the synthesis of the following: · N-(4-methoxyphenyl)-1-methyl-1H-imidazol-2-amine via C-N coupling with p-anisidine · 1,2-bis[2-methyl-5-(1-methyl-1H-imidazol-2-yl)-3-thienyl]-cyclopentene, a ligand

Application 2-Bromo-4&#8242-nitroacetophenone was used to study the pKa of the histidine-34 imidazole .