69741-66-8 Usage
Uses
Used in Pharmaceutical Synthesis:
3-METHOXY-6-NITRO-TRIFLUOROMETHYL-PHENOL is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 3-METHOXY-6-NITRO-TRIFLUOROMETHYL-PHENOL is utilized as a starting material for the production of various agrochemicals, potentially enhancing crop protection and yield.
Used as an Antibacterial Agent:
3-METHOXY-6-NITRO-TRIFLUOROMETHYL-PHENOL exhibits antibacterial properties, making it a candidate for use in applications that require the inhibition of bacterial growth, such as in medical or industrial settings.
Used as an Antifungal Agent:
3-METHOXY-6-NITRO-TRIFLUOROMETHYL-PHENOL also demonstrates antifungal properties, which can be harnessed in applications requiring the prevention of fungal growth, such as in the preservation of materials or in the treatment of fungal infections.
Check Digit Verification of cas no
The CAS Registry Mumber 69741-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,4 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69741-66:
(7*6)+(6*9)+(5*7)+(4*4)+(3*1)+(2*6)+(1*6)=168
168 % 10 = 8
So 69741-66-8 is a valid CAS Registry Number.
69741-66-8Relevant academic research and scientific papers
Process for the preparation of trifluoromethylphenols
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, (2008/06/13)
A process for the preparation of a trifluoromethylphenol or the corresponding alkoxy compound which comprises contacting a halogenobenzotrifluoride of the formula STR1 in which X denotes halogen, R1, R2 and R3 denote hydrogen, trifluoromethyl or a substituent which promotes the replacement of X by a hydroxyl group and Y denotes hydrogen, a halogen or alkoxy, at least one of the substituents R1, R2 and R3 representing a trifluoromethyl group and at least one of them representing a substituent which promotes the replacement of the radical X by a hydroxyl group, with an excess aqueous alkali metal hydroxide in an alcoholic solution in the presence of a quaternary onium salt.
