50715-86-1 Usage
Uses
Used in Pharmaceutical Industry:
[1,1-Biphenyl]-3-ol,6-methyl-(9CI) is used as a chemical intermediate for the development of various pharmaceutical products. Its unique structure allows for potential interactions with biological targets, which could be beneficial in the creation of new drugs or therapies.
Used in Polymer Production:
In the polymer industry, [1,1-Biphenyl]-3-ol,6-methyl-(9CI) may be utilized as a monomer or a component in the synthesis of polymers with specific properties. Its incorporation into polymer chains could lead to materials with enhanced characteristics, such as improved stability or functionality.
Used in Organic Synthesis:
[1,1-Biphenyl]-3-ol,6-methyl-(9CI) can be employed as a starting material or a building block in the synthesis of other organic compounds. Its reactive hydroxyl and methyl groups make it a versatile compound for further chemical modifications and the creation of a diverse range of molecules with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 50715-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50715-86:
(7*5)+(6*0)+(5*7)+(4*1)+(3*5)+(2*8)+(1*6)=111
111 % 10 = 1
So 50715-86-1 is a valid CAS Registry Number.
50715-86-1Relevant academic research and scientific papers
Atom Economical Photocatalytic Oxidation of Phenols and Site-Selective Epoxidation Toward Epoxyquinols
Péault, Louis,Planchat, Aurélien,Nun, Pierrick,Le Grognec, Erwan,Coeffard, Vincent
supporting information, p. 18192 - 18203 (2021/12/13)
The discovery of a multiple-bond-forming process merging the singlet oxygen-mediated dearomatization of 3,4-disubstitued phenols and diastereo- and regioselective epoxidation is described. This one-pot strategy using a transition metal-free multicatalytic
Copper-catalyzed oxidative aromatization of 2-cyclohexen-1-ones to phenols in the presence of catalytic hydrogen bromide under molecular oxygen
Kikushima, Kotaro,Nishina, Yuta
, p. 20150 - 20156 (2013/11/06)
Catalytic oxidative aromatization has been achieved using 2-cyclohexen-1-ones to obtain phenol derivatives in the presence of a catalytic amount of copper salt and aqueous HBr under molecular oxygen. The amount of HBr was successfully reduced to a catalytic quantity, and the other additive such as a ligand and an oxidant as well as inert conditions were unnecessary. Various mono-, di-, and trisubstituted phenols with substituents at the desired positions could be synthesized under cheap and simple conditions. An oxidative aromatization/bromination sequence was also demonstrated to obtain bromophenols with excess HBr. The Royal Society of Chemistry 2013.
