947337-17-9 Usage
Uses
Used in Asymmetric Catalysis:
(Sa)-6,6'-dibromo-1,1'-binaphthyl-2,2'-diamine is used as a ligand in asymmetric catalysis for [application reason] the creation of enantioselective catalysts. Its chiral nature allows for the selective formation of one enantiomer over the other in chemical reactions, which is crucial in the production of pharmaceuticals and other chiral molecules.
Used in Synthesis of Chiral Compounds:
In the field of organic chemistry, (Sa)-6,6'-dibromo-1,1'-binaphthyl-2,2'-diamine is used as a building block for [application reason] the synthesis of various chiral compounds. These compounds have applications in a range of industries, including pharmaceuticals, agrochemicals, and fragrances.
Used in Organic Electronics:
(Sa)-6,6'-dibromo-1,1'-binaphthyl-2,2'-diamine is also being studied for its potential applications in [application industry] organic electronics. Its unique electronic properties make it a promising candidate for use in the development of novel electronic devices, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs).
Used in Optoelectronic Devices:
Furthermore, (Sa)-6,6'-dibromo-1,1'-binaphthyl-2,2'-diamine is being explored for its potential use in [application industry] optoelectronic devices. Its optical and electronic properties could be harnessed to improve the performance of devices such as solar cells, photodetectors, and optical sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 947337-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,3,3 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 947337-17:
(8*9)+(7*4)+(6*7)+(5*3)+(4*3)+(3*7)+(2*1)+(1*7)=199
199 % 10 = 9
So 947337-17-9 is a valid CAS Registry Number.
947337-17-9Relevant academic research and scientific papers
Catalytic asymmetric benzidine rearrangement
De, Chandra Kanta,Pesciaioli, Fabio,List, Benjamin
, p. 9293 - 9295 (2013/09/12)
A chiral Br?nsted acid catalyzes the asymmetric benzidine rearrangement of N,N′-dinaphthylhydrazines. Different electronically and structurally diverse axially chiral 2,2′-binaphthyl diamine (BINAM) derivatives are obtained with high enantioselectivity. Copyright
Enantioselective Diels-Alder reaction of α-Acyloxyacroleins catalyzed by chiral 1,1′-binaphthyl-2,2′-diammonium salts
Sakakura, Akira,Suzuki, Kenji,Ishihara, Kazuaki
, p. 2457 - 2465 (2007/10/03)
A diammonium salt of chiral 1,1′-binaphthyl-2,2′-diamine (2a) and trifluoromethanesulfonimide (Tf2NH) shows excellent catalytic activity and enantioselectivity for the Diels-Alder reaction of α-acyloxyacroleins. For example, in the presence of
