57944-44-2 Usage
Uses
Since the provided materials do not contain specific information about the uses of 2-Naphthalenol,7-ethoxy-(9CI), it is not possible to list its applications according to the materials. However, it is important to note that the potential uses of 2-Naphthalenol,7-ethoxy-(9CI) may vary across different industries, and further research or consultation with scientific resources and professionals would be necessary to determine its applications and application reasons.
Check Digit Verification of cas no
The CAS Registry Mumber 57944-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,4 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57944-44:
(7*5)+(6*7)+(5*9)+(4*4)+(3*4)+(2*4)+(1*4)=162
162 % 10 = 2
So 57944-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O2/c1-2-14-12-6-4-9-3-5-11(13)7-10(9)8-12/h3-8,13H,2H2,1H3
57944-44-2Relevant academic research and scientific papers
Organocatalytic Enantioselective Synthesis of Atropisomeric Aryl-p-Quinones: Platform Molecules for Diversity-Oriented Synthesis of Biaryldiols
Chen, Ye-Hui,Li, Heng-Hui,Li, Shaoyu,Tan, Bin,Xiang, Shao-Hua,Zhang, Xiao
, p. 11374 - 11378 (2020/05/25)
Presented here is a class of novel axially chiral aryl-p-quinones as platform molecules for the preparation of non-C2 symmetric biaryldiols. Two sets of aryl-p-quinone frameworks were synthesized with remarkable enantiocontrol by means of chiral phosphoric acid catalyzed enantioselective arylation of p-quinones by central-to-axial chirality conversion. These aryl-p-quinones were then used to access a wide spectrum of highly functionalized non-C2 symmetric biaryldiols with excellent retention of the enantiopurity.
