715-31-1 Usage
General Description
2-(Pentafluorophenyl)-2-propanol is a chemical compound with the molecular formula C9H7F5O. It is a colorless liquid that is primarily used as a reagent in organic synthesis. It is often utilized as a chiral building block in the synthesis of pharmaceuticals and agrochemicals due to its ability to selectively control the stereochemistry of the final product. 2-(PENTAFLUOROPHENYL)-2-PROPANOL is also used as a solvent in various chemical reactions and as a precursor for the synthesis of other important chemicals. Additionally, it has been investigated for its potential use as a ligand in catalytic processes. However, it is important to handle this compound with care as it can be hazardous if not used properly.
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.
