40105-91-7 Usage
Uses
Used in Pharmaceutical Applications:
[5-(3-NITRO-PHENYL)-FURAN-2-YL]-METHANOL is used as a potential candidate in the pharmaceutical industry for drug development due to its furan and nitro-containing structures, which are often utilized in the creation of new drugs.
Used in Organic Synthesis:
In the field of organic chemistry, [5-(3-NITRO-PHENYL)-FURAN-2-YL]-METHANOL is used as a building block for the synthesis of more complex organic compounds, taking advantage of its phenyl group and other functional groups.
Used in Chemical Research:
[5-(3-NITRO-PHENYL)-FURAN-2-YL]-METHANOL is also used as a subject of study in chemical research, where its properties, reactivity, and potential applications are explored and documented for future reference and development.
Check Digit Verification of cas no
The CAS Registry Mumber 40105-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,0 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40105-91:
(7*4)+(6*0)+(5*1)+(4*0)+(3*5)+(2*9)+(1*1)=67
67 % 10 = 7
So 40105-91-7 is a valid CAS Registry Number.
40105-91-7Relevant academic research and scientific papers
Palladium-catalysed direct arylation of heteroaromatics bearing unprotected hydroxyalkyl functions using aryl bromides
Roger, Julien,Pozgan, Franc,Doucet, Henri
experimental part, p. 696 - 710 (2010/06/19)
Heteroaromatics bearing unprotected hydroxyalkyl functions can be arylated using aryl or heteroaryl bromides, via palladium-catalysed carbonhydrogen bond activation/arylation. Good yields were generally obtained using 0.01-0.5 mol% of the air-stable palladium acetate complex as the catalyst. The nature of the base was found to be crucial for the selectivity of this reaction. Potassium acetate led to the direct arylation products whereas caesium car-bonate led to the formation of the ether. This procedure is certainly more atom-economic than other methods for the preparation of such compounds, as no protection/ deprotection sequence of the hydroxyalkyl function and no preparation of an organometallic derivative is required.
