344402-87-5 Usage
Description
(1S,2S)-N',N'-dimethyl-1,2-diphenyl-1,2-ethanediamine is a chiral aromatic amine compound with two chiral centers, allowing it to exist in four stereoisomeric forms. It is known for its compact structure and ability to form coordination complexes, making it a valuable tool in chemical research and pharmaceutical development.
Uses
Used in Asymmetric Synthesis and Catalysis:
(1S,2S)-N',N'-dimethyl-1,2-diphenyl-1,2-ethanediamine is used as a ligand in asymmetric synthesis and catalysis, particularly in the field of organometallic chemistry. Its unique chiral properties enable it to facilitate selective reactions and improve the efficiency of catalytic processes.
Used in Pharmaceutical Development:
(1S,2S)-N',N'-dimethyl-1,2-diphenyl-1,2-ethanediamine has been studied for its potential use in the treatment of various diseases. Its ability to form coordination complexes with metal ions makes it a promising candidate for the development of new pharmaceutical agents.
Used in Material Science:
(1S,2S)-N',N'-dimethyl-1,2-diphenyl-1,2-ethanediamine is also utilized in the development of new materials. Its compact structure and coordination complex-forming ability contribute to the creation of advanced materials with unique properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 344402-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,4,0 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 344402-87:
(8*3)+(7*4)+(6*4)+(5*4)+(4*0)+(3*2)+(2*8)+(1*7)=125
125 % 10 = 5
So 344402-87-5 is a valid CAS Registry Number.
344402-87-5Relevant articles and documents
Design and development of bioinspired guanine-based organic catalyst for asymmetric catalysis
Suez, Gal,Bloch, Victoria,Nisnevich, Gennady,Gandelman, Mark
supporting information; scheme or table, p. 2118 - 2122 (2012/06/01)
Design, preparation, and studies of a family of new organic catalysts are presented. The design of the catalysts is inspired by the ability of DNA nucleobases to develop precise and explicit hydrogen bonds. We have shown that this phenomenon can be used to create a useful organic catalyst that demonstrates a recognition pattern similar to those of common organic substrates. A selected bifunctional catalyst based on a guanine structure has been shown to catalyze the conjugate addition of 1,3-dicarbonyl compounds to various nitroalkenes, providing the products in good yields and enantioselectivities.
