1960-55-0 Usage
Chemical structure
Fluorophenyl group attached to a methylpropan-2-ol group
Type of alcohol
Secondary alcohol
Explanation
Secondary alcohols have a hydroxyl (OH) group attached to a carbon atom that is bonded to two other carbon atoms. In this case, the hydroxyl group is attached to the second carbon of the methylpropan-2-ol group.
Explanation
1-(2-fluorophenyl)-2-Methylpropan-2-ol is used as a building block or starting material in the production of various pharmaceuticals and organic intermediates, which are essential for the development of new drugs and chemicals.
Explanation
As with many chemicals, it is important to handle 1-(2-fluorophenyl)-2-Methylpropan-2-ol carefully to avoid exposure and potential health risks. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be followed.
Applications
Synthesis of pharmaceuticals and organic intermediates
Potential applications
Organic chemistry and biochemistry
Safety precautions
Handle with caution due to potential health hazards
Check Digit Verification of cas no
The CAS Registry Mumber 1960-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1960-55:
(6*1)+(5*9)+(4*6)+(3*0)+(2*5)+(1*5)=90
90 % 10 = 0
So 1960-55-0 is a valid CAS Registry Number.
1960-55-0Relevant academic research and scientific papers
Amos, Stephanie G. E.,Cavalli, Diana,Le Vaillant, Franck,Waser, Jerome
, p. 23827 - 23834 (2021)
Ethynylbenziodoxolones (EBXs) are commonly used as radical traps in photocatalytic alkynylations. Herein, we report that aryl-substituted EBX reagents can be directly activated by visible light irradiation. They act as both oxidants and radical traps, alleviating the need for a photocatalyst in several reported EBX-mediated processes, including decarboxylative and deboronative alkynylations, the oxyalkynylation of enamides and the C?H alkynylation of THF. Furthermore, the method could be applied to the synthesis of alkynylated quaternary centers from tertiary alcohols via stable oxalate salts and from tertiary amines via aryl imines. A photocatalytic process using 4CzIPN as an organic dye was also developed for the deoxyalkynylation of oxalates.
