908848-70-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,4-Bis-trifluoromethyl-phenol is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to be incorporated into complex molecular structures, enhancing the activity and selectivity of the final products.
Used in Organic Synthesis:
As a reagent, 2,4-Bis-trifluoromethyl-phenol is utilized in organic synthesis to facilitate specific chemical reactions due to its strong acidity, which can be advantageous in certain synthetic pathways.
Used in Antimicrobial and Antifungal Applications:
2,4-Bis-trifluoromethyl-phenol is used as an antimicrobial and antifungal agent, leveraging its reported properties to combat microbial growth, which can be beneficial in various applications such as in medical, industrial, or environmental settings.
However, it is important to handle 2,4-Bis-trifluoromethyl-phenol with care due to its potential hazards to human health and the environment. Proper safety measures should be implemented during its use and disposal to mitigate any risks associated with 2,4-Bis-trifluoromethyl-phenol.
Check Digit Verification of cas no
The CAS Registry Mumber 908848-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,8,4 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 908848-70:
(8*9)+(7*0)+(6*8)+(5*8)+(4*4)+(3*8)+(2*7)+(1*0)=214
214 % 10 = 4
So 908848-70-4 is a valid CAS Registry Number.
908848-70-4Relevant academic research and scientific papers
Decarboxylative Hydroxylation of Benzoic Acids
Ritter, Tobias,Su, Wanqi,Xu, Peng
, p. 24012 - 24017 (2021/10/06)
Herein, we report the first decarboxylative hydroxylation to synthesize phenols from benzoic acids at 35 °C via photoinduced ligand-to-metal charge transfer (LMCT)-enabled radical decarboxylative carbometalation. The aromatic decarboxylative hydroxylation is synthetically promising due to its mild conditions, broad substrate scope, and late-stage applications.
NEW COMPOUNDS, METHODS FOR THEIR PREPARATION AND USE THEREOF
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Page/Page column 15, (2008/12/08)
A compound of formula (I) wherein X is CH=CH, CH 2O wherein the oxygen atom is bound to ring B or OCH 2wherein the oxygen atom is bound to ring A; Y is hydrogen, straight or branched C1-C6 alkyl or a pharmaceutically acceptable inorg
