175359-13-4 Usage
Chemical structure
Cyclohexadiene ring with hydroxyl groups at the 1 and 4 positions, and fluorine atoms at the 3 and 5 positions.
The cyclohexadiene ring is a six-membered carbon ring with two double bonds, and the hydroxyl and fluorine groups are attached to specific carbon atoms.
Type of compound
Diol
The compound contains two hydroxyl (-OH) groups, which classify it as a diol.
Application
Organic chemistry and pharmaceutical research
It is used as a building block for the synthesis of various compounds and pharmaceuticals.
Unique chemical structure
Valuable tool for the development of new molecules with potential biological activity.
The specific arrangement of atoms and functional groups in the molecule allows for the creation of novel compounds with potential applications in various fields.
Presence of fluorine atoms
Imparts specific chemical and pharmacological properties.
The fluorine atoms in the molecule can influence the compound's reactivity, stability, and interaction with biological targets, making it of interest in drug discovery and development.
Interest in drug discovery
Potential for the development of new pharmaceuticals.
The unique properties of the compound, including the presence of fluorine atoms, make it a promising candidate for the development of new drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 175359-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,3,5 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175359-13:
(8*1)+(7*7)+(6*5)+(5*3)+(4*5)+(3*9)+(2*1)+(1*3)=154
154 % 10 = 4
So 175359-13-4 is a valid CAS Registry Number.
175359-13-4Relevant articles and documents
Kinetics and mechanisms of the photolytic and OH° radical induced oxidation of fluorinated aromatic compounds in aqueous solutions
Karpel vel Leitner,Gombert,Ben Abdessalem,Dore
, p. 893 - 906 (2007/10/03)
Laboratory experiments with H2O2/UV oxidation processes and photolysis at 253.7 nm wavelength have been carried out on dilute aqueous solutions (C0 = 0.1 to 3.0 mM) of trifluorobenzene derivatives (1,3,5-trifluorobenzene, 1,2,3 and 1,2,4-trifluorobenzene) and of α,α,α-trifluorotoluene in the presence and in the absence of dissolved oxygen. The analyses of fluoride ions content during the oxidation experiments showed that the first steps lead to the production of about 2 mol of F-/mol of trifluorobenzene decomposed and of 1 mol of F-/mol of trifluorotoluene decomposed. Kinetic studies lead to the determination of the quantum yield for the photolysis of 1,3,5-trifluorobenzene, 1,2,3 and 1,2,4-trifluorobenzene (Φ = 0.011, 0.010 and 0.015 respectively), and of trifluorotoluene (Φ = 0.015). The rate constants for the reaction of hydroxyl radicals with these molecules, determined under specific experimental conditions, were found to range from 3.7 109 to 4.9 109 M-1.s-1). GC/MS analyses carried out on extracts at different irradiation time (UV, H2O2/UV) lead to the identification of numerous by-products from trifluorobenzene and trifluorotoluene. They consist mostly in hydroxylated and dehalogenated compounds. Dimers have also been observed during photolysis. Moreover, experiments carried out under oxygen limiting conditions revealed the formation of other compounds. For each case studied, a detailed mechanism involving radical intermediates and the different reaction sequences is proposed.
