Catalog Number |
ACM4013983-2 |
CAS |
4013-98-3 |
Structure |
![{[CurrentData.Name]}](https://resource.alfa-chemistry.com/structure/4013-98-3.gif) |
Description |
1,2-Ethanediamine, N,N'-dicyclohexyl- (EDC) is an organic compound commonly used in organic synthesis, which belongs to the family of cyclic amines. EDC is a common building block for the synthesis of other organic compounds, and it is a versatile reagent for many organic transformations. EDC is also used in a wide range of scientific research applications, from drug discovery to biochemistry and physiology. |
IUPAC Name |
N,N'-dicyclohexylethane-1,2-diamine |
Molecular Weight |
224.39 g/mol |
Molecular Formula |
C14H28N2 |
Canonical SMILES |
C1CCC(CC1)NCCNC2CCCCC2 |
InChI |
InChI=1S/C14H28N2/c1-3-7-13(8-4-1)15-11-12-16-14-9-5-2-6-10-14/h13-16H,1-12H2 |
InChI Key |
JMRWVHXGVONXEZ-UHFFFAOYSA-N |
Application |
1,2-Ethanediamine, N,N'-dicyclohexyl- is widely used in scientific research as a reagent for organic transformations. It is used in a variety of fields, including drug discovery, biochemistry, and physiology. 1,2-Ethanediamine, N,N'-dicyclohexyl- is also used in a variety of lab experiments, such as the synthesis of peptides, the synthesis of polymers, and the synthesis of complex molecules. 1,2-Ethanediamine, N,N'-dicyclohexyl- has also been used in the synthesis of drugs, such as antibiotics and antifungal agents. |
GHS Pictogram |
Corrosive |
Properties |
1,2-Ethanediamine, N,N'-dicyclohexyl- has been found to have a variety of biochemical and physiological effects. It has been shown to be an effective catalyst for the synthesis of peptides and other complex molecules. It has also been found to be a potent inhibitor of protein synthesis, meaning it can prevent the formation of proteins. 1,2-Ethanediamine, N,N'-dicyclohexyl- has also been found to inhibit the activity of enzymes, meaning it can prevent the breakdown of molecules. |