Anaesthetic amidines & benzofurans & cinnamates

2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran is an analog of the anti-arrhythmic compound Amiodarone . 2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran results from O-dealkylation of the parent compound. Analogs of Amiodarone including

2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran is an analog of the anti-arrhythmic compound Amiodarone . 2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran results from O-dealkylation of the parent compound. Analogs of Amiodarone including

2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran is an analog of the anti-arrhythmic compound Amiodarone . 2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran results from O-dealkylation of the parent compound. Analogs of Amiodarone including

2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran is an analog of the anti-arrhythmic compound Amiodarone . 2-Butyl-3-(3,5-diiodo-4-hydroxybenzoyl)benzofuran results from O-dealkylation of the parent compound. Analogs of Amiodarone including

2-HYDROXY-NAPHTHALENE-1-CARBOXYLIC ACID (3-NITRO-PHENYL)-AMIDE-

Application 3-(4-Bromophenyl)-3-(trifluoromethyl)-3 H -diazirine is a Suzuki-Miyaura (S&#8722M)-compatible building block tailored for the design of photoaffinity probes (PAPs). Photoaffinity labeling (PAL) is of growing interest in chemical

Description3-(4-Bromophenyl)-3-(trifluoromethyl)-3H-diazirine is a Suzuki-Miyaura (S−M)-compatible building block tailored for the design of photoaffinity probes (PAPs). Photoaffinity labeling (PAL) is of growing interest in chemical biology and

3-HYDROXY-NAPHTHALENE-2-CARBOXYLIC ACID (2-DIMETHYLAMINO-ETHYL)-AMIDE-

Application Reagent used for Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides One-pot ipso-nitration of

Application Reagent used for Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides One-pot ipso-nitration of

4-Nitro-2-(trifluoromethyl)aniline undergoes diazotization and coupling with: · N-hydroxyalkylamino-5-napthols · pyrazolones and naptholsulphonic acids · N-(2-cyanoethyl)-N-(hydroxyalkyl)anilines.

Employed in a rhodium-catalyzed cyclization of alkynones. May contain varying amounts of anhydride.Reagent used for Ligand-free palladium-catalyzed Suzuki-Miyaura cross-couplings Ruthenium catalyzed direct arylation of benzylic sp3 carbons of