145372-06-1 Usage
General Description
[1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxy- is a chemical compound with the molecular formula C24H20O4. It is a diol compound, meaning it contains two hydroxyl groups. The presence of two naphthalene rings in the compound gives it a unique structure and properties. It is typically used as a chiral ligand in asymmetric catalysis, particularly in metal-catalyzed reactions. The dimethoxy groups attached to the naphthalene rings help to stabilize the compound and can affect its solubility and reactivity. [1,1'-Binaphthalene]-2,2'-diol, 6,6'-dimethoxy- is commonly used in organic synthesis and pharmaceutical research due to its ability to facilitate enantioselective reactions.
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
