885268-02-0 Usage
Description
5-Trifluoromethyl-1-tetralone, also known as 5-TFMT, is a fluorinated organic compound belonging to the class of tetralone derivatives. It features a trifluoromethyl group attached to the fifth position of the tetralone ring, which endows it with unique pharmacological properties.
Uses
Used in Medicinal Chemistry:
5-Trifluoromethyl-1-tetralone is used as a compound in medicinal chemistry for its antioxidant, anti-inflammatory, and neuroprotective activities. These properties make it a promising candidate for the development of novel pharmaceuticals.
Used in Drug Discovery:
In the field of drug discovery, 5-TFMT is utilized for its potential to contribute to the creation of new medications. Its pharmacological properties are being studied for the treatment of various diseases, highlighting its value in pharmaceutical research.
Used in Pharmaceutical Development:
5-Trifluoromethyl-1-tetralone is employed as a key component in the development of novel pharmaceuticals targeting a range of diseases. Its unique structure and properties allow it to be a valuable asset in designing effective treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 885268-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,6 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 885268-02:
(8*8)+(7*8)+(6*5)+(5*2)+(4*6)+(3*8)+(2*0)+(1*2)=210
210 % 10 = 0
So 885268-02-0 is a valid CAS Registry Number.
885268-02-0Relevant articles and documents
Highly enantioselective [3+2] coupling of cyclic enamides with quinone monoimines promoted by a chiral phosphoric acid
Zhang, Minmin,Yu, Shuowen,Hu, Fangzhi,Liao, Yijun,Liao, Lihua,Xu, Xiaoying,Yuan, Weicheng,Zhang, Xiaomei
, p. 8757 - 8760 (2016/07/15)
Enantioselective [3+2] coupling of cyclic enamides with quinone monoimines was realised using a chiral phosphoric acid as a catalyst. This transformation allowed for the synthesis of highly enantioenriched polycyclic 2,3-dihydrobenzofurans (up to 99.9% ee). The absolute configuration of one product was determined by an X-ray crystal structural analysis. We also found a possible mechanism for this reaction.
