Antiviral drugs

2-Bromobenzaldehyde is a versatile building block used in Suzuki-Miyaura and Buchwald-Hartwig reactions, cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds Application Synthetic applications of 2-bromobenzaldehyde include:

2-Bromobenzaldehyde is a versatile building block used in Suzuki-Miyaura and Buchwald-Hartwig reactions, cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds Application Synthetic applications of 2-bromobenzaldehyde include:

2-Bromobenzoic acid (2-BA) on condensation with aminoquinolines yields phenylquinolylamines. 2-BA is the common building block for synthesis of various nitrogen heterocycles.

2-Bromobenzoic acid (2-BA) on condensation with aminoquinolines yields phenylquinolylamines. 2-BA is the common building block for synthesis of various nitrogen heterocycles.

2-Bromobenzoic acid (2-BA) on condensation with aminoquinolines yields phenylquinolylamines. 2-BA is the common building block for synthesis of various nitrogen heterocycles.

2-Bromoimidazo[2,1-b][1,3,4]thiadiazole.

2-Bromoimidazo[2,1-b][1,3,4]thiadiazole.

2-Bromoimidazo[2,1-b][1,3,4]thiadiazole.

2-Bromoimidazo[2,1-b][1,3,4]thiadiazole.

Application 2-Bromothiazole was used to N -arylate 5- and 7-azaindoles. 2-Bromothiazole was also used as starting reagent in the synthesis of: 2-cyanothiazole via cpper-catalyzed cyanation 2,4,5-trisubstituted thiazoles novel electron-deficient

Usually used to N-arylate 5- and 7-azaindoles.And also used as starting reagent in the synthesis of 2-cyanothiazole via cpper-catalyzed cyanation,2,4,5-trisubstituted thiazoles,novel electron-deficient fused

Usually used to N-arylate 5- and 7-azaindoles.And also used as starting reagent in the synthesis of 2-cyanothiazole via cpper-catalyzed cyanation,2,4,5-trisubstituted thiazoles,novel electron-deficient fused