715-31-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2-(PENTAFLUOROPHENYL)-2-PROPANOL is used as a chiral building block for the synthesis of enantiomerically pure compounds, which is essential in creating pharmaceuticals and agrochemicals with specific biological activities. Its ability to control stereochemistry ensures the production of desired enantiomers, contributing to the effectiveness and safety of these products.
Used in Organic Synthesis:
As a reagent, 2-(PENTAFLUOROPHENYL)-2-PROPANOL is utilized in various organic synthesis processes, facilitating the formation of complex organic molecules. Its properties make it a valuable component in the creation of a wide range of chemical compounds.
Used as a Solvent:
In the chemical industry, 2-(PENTAFLUOROPHENYL)-2-PROPANOL serves as a solvent for different chemical reactions. Its solvent properties can influence the rate and yield of reactions, making it a useful tool in the synthesis of various compounds.
Used in the Synthesis of Other Chemicals:
2-(PENTAFLUOROPHENYL)-2-PROPANOL is also employed as a precursor in the synthesis of other important chemicals, highlighting its versatility and importance in the chemical manufacturing process.
Used in Catalytic Processes:
It has been investigated for its potential use as a ligand in catalytic processes, where it could enhance the efficiency and selectivity of catalytic reactions, contributing to advancements in chemical synthesis and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 715-31-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 715-31:
(5*7)+(4*1)+(3*5)+(2*3)+(1*1)=61
61 % 10 = 1
So 715-31-1 is a valid CAS Registry Number.
715-31-1Relevant articles and documents
Photosubstitution reactions on aromatic and heteroaromatic rings evidence for addition and substitution mechanism
Sket, Boris,Zupan, Marko,Zupancic, Natasa,Pahor, Barbara
, p. 5029 - 5042 (2007/10/02)
Irradiation of a cyclohexane solution of hexafluorobenzene in the presence of benzophenone resulted in both, substitution and addition products. Similar photoreaction has been observed by irradiation of hexafluorobenzene in some alcohols in the presence of benzophenone. The reaction of pentafluorobenzene with methanol or cyclohexane resulted in the substitution of a 2-or 4-fluoro atom, while the reaction of pentafluoroanisole resulted in the formation of o-, m- and p-isomers. Irradiation of a cyclohexane solution or of an alcohol solution of octafluoronaphthalene yielded 1- and 2-substituted products. On the other hand, the photosubstitution of fluorine atom in pentafluoropyridine took place exclusively at the position four, thus forming 4-cyclohexyl or 4-(1-hydroxyalkyl) substituted products.
