(1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine

Catalog Number	ACM425615425-2
CAS	425615-42-5
Structure
Description	(1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine, or (1R,2R)-BTE, is a symmetrical diamine compound with a molecular formula of C16H24N2. It is a colorless, water-soluble liquid with a faint odor and a melting point of -51°C. In recent years, (1R,2R)-BTE has gained popularity in the scientific community due to its unique properties and its potential applications in a variety of scientific research fields. This paper will discuss the synthesis method of (1R,2R)-BTE, its scientific research applications, the mechanism of action, its biochemical and physiological effects, the advantages and limitations for lab experiments, and the potential future directions of its research.
IUPAC Name	(1R,2R)-1,2-bis(2,4,6-trimethylphenyl)ethane-1,2-diamine
Molecular Weight	296.4 g/mol
Molecular Formula	C20H28N2
Canonical SMILES	CC1=CC(=C(C(=C1)C)C(C(C2=C(C=C(C=C2C)C)C)N)N)C
InChI	InChI=1S/C20H28N2/c1-11-7-13(3)17(14(4)8-11)19(21)20(22)18-15(5)9-12(2)10-16(18)6/h7-10,19-20H,21-22H2,1-6H3/t19-,20-/m1/s1
InChI Key	ILMRHFMYIXTNMC-WOJBJXKFSA-N
Application	((1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine)-BTE has been found to have a wide range of scientific research applications. It has been used as a catalyst in the synthesis of organic compounds, as a reagent in the synthesis of polymers, and as a ligand in the synthesis of coordination compounds. It has also been used as a chromatographic stationary phase for the separation of mixtures of organic compounds, and as a reagent in the synthesis of pharmaceuticals. In addition, ((1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine)-BTE has been used as a surfactant in the synthesis of nanomaterials, and as a reactant in the synthesis of polymers for biomedical applications.
GHS Pictogram	Irritant
Isomeric SMILES	CC1=CC(=C(C(=C1)C)[C@H]([C@@H](C2=C(C=C(C=C2C)C)C)N)N)C
Properties	The biochemical and physiological effects of ((1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine)-BTE are not fully understood. However, in vitro studies have shown that the compound has a low toxicity and does not induce any adverse effects when administered in animal models. In addition, the compound has been shown to have anti-inflammatory and antioxidant properties, and to possess antifungal activity.