1701-20-8 Usage
Uses
Used in Pharmaceutical Industry:
4-HYDROXY-6-METHYL-2-(TRIFLUOROMETHYL)QUINOLINE is used as a potential pharmaceutical compound for its unique structure and properties. It may contribute to the development of new drugs, particularly in the area of medicinal chemistry, where its electronegative trifluoromethyl group and hydroxyl functionality could offer novel therapeutic effects.
Used in Research and Development:
In the field of scientific research, 4-HYDROXY-6-METHYL-2-(TRIFLUOROMETHYL)QUINOLINE serves as a valuable research reagent. It aids in the study of quinoline derivatives, providing insights into the structure-activity relationships and potential applications of related compounds in various biological and chemical processes.
Further studies may be necessary to understand the full scope of 4-HYDROXY-6-METHYL-2-(TRIFLUOROMETHYL)QUINOLINE's applications and effects, ensuring its safe and effective use in relevant industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1701-20-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1701-20:
(6*1)+(5*7)+(4*0)+(3*1)+(2*2)+(1*0)=48
48 % 10 = 8
So 1701-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H8F3NO/c1-6-2-3-8-7(4-6)9(16)5-10(15-8)11(12,13)14/h2-5H,1H3,(H,15,16)
1701-20-8Relevant academic research and scientific papers
2 -trifluoromethyl -4 - amino - quinoline derivative and application thereof
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Paragraph 0032-0036; 0140-0144, (2021/11/10)
The invention discloses 2 -trifluoromethyl -4 - amino - quinoline derivatives and application thereof, and comprises a compound represented by the following general formula I. The prepared compound is used for preparing an anti-tumor active drug, has a go
A convenient synthesis of 2-(F-alkyl)-4-hydroxyquinolines
Huang, Wei-Yuan,Liu, Yan-Song,Lu, Long
, p. 209 - 214 (2007/10/02)
A convenient new route to 2-(F-alkyl)-4-hydroxyquinolines has been developed.In the presence of triethylamine, treatment of ethyl 2,2-dihydropolyfluoroalkanoates with aromatic amines in acetonitrile at 70 deg C led to a mixture of the corresponding enamin
