Central nervous system drugs

N，N’-Dimethyl-1，4-butanediamine.

N，N’-Dimethyl-1，4-butanediamine.

N，N’-Dimethyl-1，4-butanediamine.

Application N,N &#8242-Dimethylethylenediamine was used to enhance CO 2 adsorption. It was incorporated into H 3 [(Cu 4 Cl) 3 (BTTri) 8 (CuBTTri H 3 BTTri = 1,3,5-tri(1 H -1,2,3-triazol-4-yl)benzene), a water-stable, triazolate-bridged framework,

Application N,N &#8242-Dimethylethylenediamine was used to enhance CO 2 adsorption. It was incorporated into H 3 [(Cu 4 Cl) 3 (BTTri) 8 (CuBTTri H 3 BTTri = 1,3,5-tri(1 H -1,2,3-triazol-4-yl)benzene), a water-stable, triazolate-bridged framework,

Application N , N &#8242-Dimethylethylenediamine can be used as a ligand in the following processes: Copper-catalyzed cyanations of aryl bromides using potassium hexacyanoferrate(II) to form the corresponding benzonitriles. Copper-catalyzed tandem

Application N , N &#8242-Dimethylethylenediamine can be used as a ligand in the following processes: Copper-catalyzed cyanations of aryl bromides using potassium hexacyanoferrate(II) to form the corresponding benzonitriles. Copper-catalyzed tandem

Application N , N &#8242-Dimethylethylenediamine can be used as a ligand in the following processes: Copper-catalyzed cyanations of aryl bromides using potassium hexacyanoferrate(II) to form the corresponding benzonitriles. Copper-catalyzed tandem

Application N , N &#8242-Dimethylethylenediamine can be used as a ligand in the following processes: Copper-catalyzed cyanations of aryl bromides using potassium hexacyanoferrate(II) to form the corresponding benzonitriles. Copper-catalyzed tandem

N,N'-Dimethylphthalamide.

N,N'-Dimethylphthalamide.

N,N'-Dimethylthiourea