80172-04-9 Usage
General Description
3,4,5-Trifluorobenzotrifluoride is a chemical compound with the molecular formula C7H3F6. It is a colorless liquid that is mainly used in the production of pharmaceuticals, agrochemicals, and electronic materials. This chemical is highly flammable and may be harmful if inhaled, ingested, or absorbed through the skin. It is also a strong irritant to the eyes, skin, and respiratory system. 3,4,5-Trifluorobenzotrifluoride may also be harmful to aquatic life and should be handled and disposed of with caution. It is important to follow proper safety protocols when working with this chemical to minimize the risk of adverse health effects or environmental contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 80172-04-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80172-04:
(7*8)+(6*0)+(5*1)+(4*7)+(3*2)+(2*0)+(1*4)=99
99 % 10 = 9
So 80172-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H2F6/c8-4-1-3(7(11,12)13)2-5(9)6(4)10/h1-2H
80172-04-9Relevant articles and documents
Au@ZnO Core-Shell: Scalable Photocatalytic Trifluoromethylation Using CF3CO2Na as an Inexpensive Reagent under Visible Light Irradiation
Bazyar, Zahra,Hosseini-Sarvari, Mona
supporting information, p. 2345 - 2353 (2019/10/16)
Trifluoromethylation is of significant importance for the synthesis of many small molecules vital for medicinal and agrochemical research. The importance of the CF3 group as well as the related synthetic challenges is so evident that many reagents have been reported for the synthesis of trifluoromethylated compounds, but these typical reagents are expensive and the methods for preparing them are difficult. Here, we report a new scalable and operationally simple trifluoromethylation reaction using sodium trifluoroacetate as a reagent and Au-modified ZnO as a photocatalyst under visible light irradiation. The reaction proceeds via trifluoromethylation of a broad range of aryl halides, arylboronic acids, and arene and heteroarene substrates. Some pharmaceutical and agrochemical compounds have been trifluoromethylated directly to demonstrate the applicability of the method.