3002-30-0 Usage
Description
Methyl 9H-fluorene-9-carboxylate is an organic compound with the molecular formula C15H12O2. It is a derivative of fluorene, a polycyclic aromatic hydrocarbon, and features a carboxylate group attached to the 9-position of the fluorene ring. methyl 9H-fluorene-9-carboxylate is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Chemical Synthesis:
Methyl 9H-fluorene-9-carboxylate is used as an intermediate in the synthesis of 2-Methylfluoranthene (M305305), which is an environmental pollutant known to cause oxidative DNA damage in humans. methyl 9H-fluorene-9-carboxylate plays a crucial role in the production process, contributing to the formation of the final product.
Used in Environmental Research:
Methyl 9H-fluorene-9-carboxylate is used as a research compound in the field of environmental science. It helps scientists understand the effects of environmental pollutants on human health, particularly in the context of oxidative DNA damage. This knowledge is essential for developing strategies to mitigate the harmful effects of such pollutants.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, methyl 9H-fluorene-9-carboxylate could potentially be used in the pharmaceutical industry as a building block for the development of new drugs. Its unique chemical structure may offer opportunities for the creation of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 3002-30-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3002-30:
(6*3)+(5*0)+(4*0)+(3*2)+(2*3)+(1*0)=30
30 % 10 = 0
So 3002-30-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H12O2/c1-17-15(16)14-12-8-4-2-6-10(12)11-7-3-5-9-13(11)14/h2-9,14H,1H3
3002-30-0Relevant articles and documents
EQUILIBRIUM NH ACIDITY OF POLYFLUOROALKYL-CONTAINIG COMPOUNDS
Vlasov, V. M.,Terekhova, M. I.,Petrov, E. S.,Shatenshtein, A. I.,Yakobson, G. G.
, p. 1807 - 1813 (2007/10/02)
The pK vvalues of NH acids containing a polyfluoroaryl group at the α position to the acid center (polyfluoroalkyl- and diarylamines, polyfluoroanilines) with reference to 9-phenylfluorene were obtained by transmetallation in dimethyl sulfoxide (cation potassium).The acidifying effects of the C6F5, β-C10F7, and C5F4N (tetrafluoro-4-pyridyl) groups were evaluated.The acidity of the C6F5NHR compounds correlates satisfactorily with the parameters of the 19F NMR spectra of the N-anions or NH acids and with the ?* constants of the substituent R.In the series of compounds p-RC6F4NHC6F5 and p-RC6F4NH(O)C6H5 a correlation is observed between the pK values and the Hammett constants of the substituent R.In most cases the conduction of the effect of the substituent R in these series to the NH reaction center is analogous with that in the corresponding unfluorinated series.
