795274-69-0 Usage
Five-membered aromatic ring
1H-Pyrrole, 2-[3,5-bis(trifluoromethyl)phenyl]has a ring structure with five atoms, including one nitrogen atom, which gives it aromatic properties.
Trifluoromethyl groups
The compound contains two trifluoromethyl (CF3) groups each consisting of one carbon atom bonded to three fluorine atoms attached to a phenyl ring.
Derivative of pyrrole
1H-Pyrrole, 2-[3,5-bis(trifluoromethyl)phenyl]is derived from pyrrole, a basic five-membered aromatic ring with one nitrogen atom.
Building block in organic synthesis
This chemical is commonly used as a building block in the creation of more complex organic compounds.
Pharmaceutical development
The compound is also used in the development of pharmaceuticals, due to its potential to form a variety of biologically active compounds.
Potential toxicity and reactivity
1H-Pyrrole, 2-[3,5-bis(trifluoromethyl)phenyl]may be toxic or reactive, so it is important to handle it with care and follow proper safety precautions.
Check Digit Verification of cas no
The CAS Registry Mumber 795274-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,5,2,7 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 795274-69:
(8*7)+(7*9)+(6*5)+(5*2)+(4*7)+(3*4)+(2*6)+(1*9)=220
220 % 10 = 0
So 795274-69-0 is a valid CAS Registry Number.
795274-69-0Relevant academic research and scientific papers
Sensitization-Initiated Electron Transfer for Photoredox Catalysis
Ghosh, Indrajit,Shaikh, Rizwan S.,K?nig, Burkhard
supporting information, p. 8544 - 8549 (2017/07/11)
Photosynthetic organisms exploit antenna chromophores to absorb light and transfer excitation energy to the reaction center where redox reactions occur. In contrast, in visible-light chemical photoredox catalysis, a single species (i.e., the photoredox catalyst) absorbs light and performs the redox chemistry. Mimicking the energy flow of the biological model, we report a two-center photoredox catalytic approach in which the tasks of light energy collection and electron transfer (i.e., redox reactions) are assigned to two different molecules. Ru(bpy)3Cl2 absorbs the visible light and transfers the energy to polycyclic aromatic hydrocarbons that enable the redox reactions. This operationally simple sensitization-initiated electron transfer enables the use of arenes that do not absorb visible light, such as anthracene or pyrene, for photoredox applications. We demonstrate the merits of this approach by the reductive activation of chemical bonds with high reduction potentials for carbon–carbon and carbon–heteroatom bond formations.
