179337-54-3 Usage
Uses
Used in Asymmetric Catalysis:
(1S,2S)-1,2-Dicyclohexylethane-1,2-diamine is utilized as a ligand in asymmetric catalysis, where it plays a pivotal role in facilitating enantioselective reactions, leading to the production of chiral compounds with specific three-dimensional arrangements.
Used in Pharmaceutical and Agrochemical Synthesis:
In the pharmaceutical and agrochemical industries, (1S,2S)-1,2-Dicyclohexylethane-1,2-diamine serves as a building block for the creation of chiral molecules, which are essential in the development of drugs and agrochemicals with targeted biological activities.
Used in Polymer and Resin Production:
(1S,2S)-1,2-Dicyclohexylethane-1,2-diamine is employed as a curing agent in the production of polymers and resins, specifically for epoxy resins. Its application ensures the formation of strong, thermosetting materials with a wide range of applications in various industries.
Used in Chemical Manufacturing:
The unique structure and properties of (1S,2S)-1,2-Dicyclohexylethane-1,2-diamine make it a valuable component in the broader field of chemical manufacturing, where it contributes to the synthesis of a variety of organic compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 179337-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,3,3 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 179337-54:
(8*1)+(7*7)+(6*9)+(5*3)+(4*3)+(3*7)+(2*5)+(1*4)=173
173 % 10 = 3
So 179337-54-3 is a valid CAS Registry Number.
179337-54-3Relevant academic research and scientific papers
Enantioselective Reductive Coupling of Imines Templated by Chiral Diboron
Chen, Dongping,Li, Kaidi,Tang, Wenjun,Xu, Guangqing,Xu, Ronghua,Zhou, Mingkang
supporting information, p. 10337 - 10342 (2020/07/04)
We herein report a general, practical, and highly efficient method for asymmetric synthesis of a wide range of chiral vicinal diamines via reductive coupling of imines templated by chiral diboron. The protocol features high enantioselectivity and stereospecificity, mild reaction conditions, simple operating procedures, use of readily available starting materials, and a broad substrate scope. The method signifies the generality of diboron-enabled [3,3]-sigmatropic rearrangement.
Synthesis of phosphoramides for the lewis base-catalyzed allylation and aldol addition reactions
Denmark, Scott E.,Su, Xiping,Nishigaichi, Yutaka,Coe, Diane M.,Wong, Ken-Tsung,Winter, Stephen B. D.,Choi, Jun Young
, p. 1958 - 1967 (2007/10/03)
Both chiral and achiral phosphoramides of diverse structure were prepared from diamines by the coupling to phosphorus(V) or phosphorus(III) reagents. Several enantiopure 1,2-diphenyl-1,2-ethanediamine analogues have been prepared by the reductive coupling of the corresponding N-silylimine with NbCl4(THF)2 and subsequent resolution by the formation of diastereomeric menthyl carbamates. (S,S)-N,N'-Di-(1-naphthyl)-1,2-diphenyl- 1,2-ethanediamine 15 was prepared by the arylation of (S,S)-1,2-diphenyl- 1,2-ethanediamine with naphthyl iodide.
