145372-06-1 Usage
Description
[1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxyis a unique chemical compound with the molecular formula C24H20O4. It is a diol compound, characterized by the presence of two hydroxyl groups. The distinctive feature of this compound is the incorporation of two naphthalene rings, which endows it with a specific structure and a range of properties. The dimethoxy groups attached to the naphthalene rings not only contribute to the stabilization of the compound but also influence its solubility and reactivity. [1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxyis predominantly utilized as a chiral ligand in asymmetric catalysis, especially in metal-catalyzed reactions, and is highly valued in organic synthesis and pharmaceutical research for its capacity to enable enantioselective reactions.
Uses
Used in Pharmaceutical Research:
[1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxyis used as a chiral ligand for [facilitating enantioselective reactions] in pharmaceutical research. Its unique structure allows for the creation of enantiomerically pure compounds, which is crucial for the development of drugs with specific biological activities and reduced side effects.
Used in Organic Synthesis:
In the field of organic synthesis, [1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxyis used as a chiral catalyst for [asymmetric catalysis], particularly in metal-catalyzed reactions. [1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxy-'s ability to selectively catalyze reactions with a preference for one enantiomer over the other is invaluable for synthesizing complex organic molecules with desired stereochemistry.
Used in Asymmetric Catalysis:
[1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxyis employed as a chiral auxiliary in [asymmetric catalysis] to enhance the selectivity of chemical reactions. Its presence can significantly improve the yield of desired enantiomers, which is essential for the production of high-purity compounds in various industries, including pharmaceuticals, agrochemicals, and fragrances.
Check Digit Verification of cas no
The CAS Registry Mumber 145372-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,3,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145372-06:
(8*1)+(7*4)+(6*5)+(5*3)+(4*7)+(3*2)+(2*0)+(1*6)=121
121 % 10 = 1
So 145372-06-1 is a valid CAS Registry Number.
145372-06-1Relevant articles and documents
Enantioselective oxidative-coupling of polycyclic phenols
Takizawa, Shinobu,Kodera, Junpei,Yoshida, Yasushi,Sako, Makoto,Breukers, Stefanie,Enders, Dieter,Sasai, Hiroaki
, p. 1786 - 1793 (2014/03/21)
Enantioselective oxidative-coupling of polycyclic phenols, such as 2-anthracenol, 9- or 3-phenanthrol, and 5-chrysenol was established by using vanadium(V/IV) catalysis under air or O2 as a co-oxidant. In the vanadium catalyzed reaction, the co
