72768-94-6 Usage
General Description
2-(Difluoromethoxy)benzyl alcohol is a chemical compound that belongs to the organofluorine class of compounds, which contain a bond between carbon and fluorine. This class of compounds is known for its stability and resistance to many forms of degradation, including metabolic degradation in the human body. The exact properties of 2-(difluoromethoxy)benzyl alcohol, such as its density, boiling point, and melting point, may vary slightly depending on its exact molecular structure. It is typically used in organic synthesis as a pharmaceutical intermediate. Its hazard and safety measures are not commonly reported, suggesting that it is not highly toxic or dangerous under normal handling procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 72768-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,6 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72768-94:
(7*7)+(6*2)+(5*7)+(4*6)+(3*8)+(2*9)+(1*4)=166
166 % 10 = 6
So 72768-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F2O2/c9-8(10)12-7-4-2-1-3-6(7)5-11/h1-4,8,11H,5H2
72768-94-6Relevant articles and documents
Synthesis of Phenanthridines through Palladium-Catalyzed Cascade Reaction of 2-Halo-N-Ms-arylamines with Benzyl Halides/Sulfonates
Yang, Si-Yi,Han, Wen-Yong,Zhang, Ding-Lei,Zhou, Xiao-Jian,Bai, Mei,Cui, Bao-Dong,Wan, Nan-Wei,Yuan, Wei-Cheng,Chen, Yong-Zheng
, p. 996 - 1003 (2017/02/15)
An efficient palladium-catalyzed nucleophilic substitution/C–H activation/aromatization cascade reaction between readily available 2-halo-N-Ms-arylamines (Ms = methanesulfonyl) and benzyl halides/sulfonates has been described. A wide variety of phenanthridines were synthesized in a one-pot fashion in moderate to high yields (37–86 %). Notably, this method provides a straightforward, facile approach for the synthesis of phenanthridines. The practicality was further substantiated by successfully carrying out a gram-scale preparation.
