| Catalog Number |
ACM121788736 |
| CAS |
121788-73-6 |
| Structure |
 |
| Description |
(R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine, also known as BTE, is an organic compound with a wide range of applications in the scientific research field. It is a trifluoromethanesulfonyl derivative of 1,2-diphenylethylenediamine, which is a type of diamine that is used in the synthesis of organic molecules. BTE is used as a catalyst and reagent in organic synthesis, and it has been extensively studied due to its unique properties. |
| Synonyms |
(R,R)-1,2-Bis(trifluoromethanesulfonamido)-1,2-diphenylethane |
| IUPAC Name |
N-[(1R,2R)-1,2-diphenyl-2-(trifluoromethylsulfonylamino)ethyl]-1,1,1-trifluoromethanesulfonamide |
| Molecular Weight |
476.4 g/mol |
| Molecular Formula |
C16H14F6N2O4S2 |
| Canonical SMILES |
C1=CC=C(C=C1)C(C(C2=CC=CC=C2)NS(=O)(=O)C(F)(F)F)NS(=O)(=O)C(F)(F)F |
| InChI |
InChI=1S/C16H14F6N2O4S2/c17-15(18,19)29(25,26)23-13(11-7-3-1-4-8-11)14(12-9-5-2-6-10-12)24-30(27,28)16(20,21)22/h1-10,13-14,23-24H/t13-,14-/m1/s1 |
| InChI Key |
XQAIGOHPAZPGOU-ZIAGYGMSSA-N |
| Melting Point |
213 °C |
| Purity |
98%+ |
| Appearance |
White to off-white powder |
| Application |
(R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine has a wide range of applications in the scientific research field. It is used as a catalyst and reagent in organic synthesis, and it has been extensively studied due to its unique properties. (R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine can be used to catalyze the reaction of carboxylic acids and alcohols to form esters, and it can also be used to catalyze the reaction of amines and carboxylic acids to form amides. (R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine has also been used in the synthesis of peptides, and it can be used to catalyze the formation of carbon-carbon bonds. Additionally, (R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine has been used as a ligand in coordination chemistry and can be used to catalyze the formation of transition metal complexes. |
| GHS Pictogram |
Irritant |
| Isomeric SMILES |
C1=CC=C(C=C1)[C@H]([C@@H](C2=CC=CC=C2)NS(=O)(=O)C(F)(F)F)NS(=O)(=O)C(F)(F)F |
| Properties |
The biochemical and physiological effects of (R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine are not well understood, however it is believed to be non-toxic and non-carcinogenic. Additionally, (R,R)-N,N'-Bis(trifluoromethanesulfonyl)-1,2-diphenylethylenediamine has been shown to have no adverse effects on the environment when used in laboratory experiments. |
