Antiseptic organometallic compounds

2,6-Diisopropylaniline is an amine. It undergoes condensation with triacetylmethane in toluene in the presence of p -toluenesulfonic acid provides 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione.

2,6-Diisopropylaniline on condensation with triacetylmethane in toluene in the presence of p -toluenesulfonic acid provides 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione. Application 2,6-Diisopropylaniline was used in the

2,6-Diisopropylaniline on condensation with triacetylmethane in toluene in the presence of p -toluenesulfonic acid provides 3-[1-(2,6-diisopropylphenylamino)ethylidene]pentane-2,4-dione. Application 2,6-Diisopropylaniline was used in the

2',3'-O-Isopropylideneinosine.

Chiral urea compounds catalyzed hetero-Michael addition reaction of 2(5 H )-furanone (&#947-crotonolactone) to pyrrolidine . The quorum sensing inhibition activity by 2(5 H )-furanone was studied using bioindicator strains .

Chiral urea compounds catalyzed hetero-Michael addition reaction of 2(5 H )-furanone (&#947-crotonolactone) to pyrrolidine . The quorum sensing inhibition activity by 2(5 H )-furanone was studied using bioindicator strains .

2,2,3,3-Tetramethylcyclopropanecarboxylic acid is an inactive cyclopropyl analog of valproic acid (major antiepileptic drug). Inhibition of histone deacetylases and tumor cells cytotoxicities of 2,2,3,3-tetramethylcyclopropanecarboxylic acid was

DescriptionThe Microtox EC50values for 2,2,4,4-tetramethyl-3-pentanone has been reported. The kinetics, stoichiometry and products of the reduction reaction of 2,2,4,4-tetramethyl-3-pentanone using lithium triethylborohydride under standard

DescriptionThe Microtox EC50values for 2,2,4,4-tetramethyl-3-pentanone has been reported. The kinetics, stoichiometry and products of the reduction reaction of 2,2,4,4-tetramethyl-3-pentanone using lithium triethylborohydride under standard

2,2′-[(1R,2R)-(-)-1,2-Cyclohexanediylbis((E)-(nitrilomethylidyne))]bis[4-(tert-butyl)-6-(4-morpholinylmethyl)phenol].

2,5-Dimethylbenzenethiol was used in the synthesis of poly(2-dodecanoylsulfanyl-p-phenylenevinylene). It was also used in the synthesis of 1,1,2-trichloro-4-(2,5-dimethylphenylthio)-1-buten-3-yne:

2,5-Dimethylbenzenethiol was used in the synthesis of poly(2-dodecanoylsulfanyl-p-phenylenevinylene). It was also used in the synthesis of 1,1,2-trichloro-4-(2,5-dimethylphenylthio)-1-buten-3-yne: