6311-22-4 Usage
Uses
Used in Pharmaceutical Industry:
9-hydroxy-9-methylfluorene serves as a key reactant in organic synthesis for the production of a variety of pharmaceuticals. Its unique chemical structure allows for the creation of diverse drug molecules, contributing to the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 9-hydroxy-9-methylfluorene is utilized as an intermediate in the synthesis of various agrochemicals. Its involvement in the production of pesticides and other agricultural chemicals aids in enhancing crop protection and yield.
Used in Dye Industry:
9-hydroxy-9-methylfluorene also finds application in the dye industry, where it is used in the synthesis of different types of dyes. Its chemical properties enable the creation of a wide range of colorants used in various industries, including textiles, plastics, and printing.
Used in Research Applications:
9-hydroxy-9-methylfluorene is employed in research settings to explore its potential anti-inflammatory and antioxidant activities. Studies on its biological effects can lead to a better understanding of its therapeutic potential and inform the development of novel treatments.
However, it is important to note that the compound's carcinogenic and mutagenic properties have been studied, indicating the need for stringent safety measures and regulatory oversight in its use and handling. This ensures that the benefits of 9-hydroxy-9-methylfluorene can be harnessed while minimizing potential health and environmental impacts.
Check Digit Verification of cas no
The CAS Registry Mumber 6311-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6311-22:
(6*6)+(5*3)+(4*1)+(3*1)+(2*2)+(1*2)=64
64 % 10 = 4
So 6311-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O/c1-14(15)12-8-4-2-6-10(12)11-7-3-5-9-13(11)14/h2-9,15H,1H3
6311-22-4Relevant academic research and scientific papers
Photooxidation of aryl alkanes by a decatungstate/triethylsilane system in the presence of molecular oxygen
Lykakis, Ioannis N.,Orfanopoulos, Michael
, p. 7645 - 7649 (2007/10/03)
Decatungstate photocatalyzes the oxidation of aryl alkanes to the corresponding tertiary hydroperoxides and alcohols, in the presence of molecular oxygen. The addition of triethylsilane to the reaction mixture substantially increases the proportion of hydroperoxide formed.
[(3-dimethylamino)propyl]dimethylaluminum: A convenient reagent for methylation and ethynylation of carbonyl compounds
Baidossi, Wael,Rosenfeld, Ayelet,Wassermann, Brigit C.,Schutte, Stefan,Schumann, Herbert,Blum, Jochanan
, p. 1127 - 1130 (2007/10/03)
At 60-80°C the title compound methylates a variety of mono- and diketones. Aromatic aldehydes undergo simple methylation by the reagent only after initial treatment with an equivalent amount of AlCl3. Upon reaction of Me2Al(CH2)3NMe2 with terminal acetylenes the aluminum complex is converted into a carbonyl-alkynylation reagent.
REACTIVITY OF CARBANIONS. XXIII. WITTIG REARRANGEMENT OF 9-FLUORENOL ETHERS UNDER THE CONDITIONS OF PHASE-TRANSFER CATALYSIS
Solov'yanov, A. A.,El-Said, Ahmed Ali Ahmed,Beletskaya, I. P.,Reutov, O. A.
, p. 1232 - 1243 (2007/10/02)
The Wittig rearrangement of the phenyl, methyl, benzyl, and allyl ethers of 9-fluorenol was investigated under the conditions of phase-transfer catalysis in a system consisting of a solid powdered base and an organic phase.With the exception of the phenyl ether, which does not enter into the reaction, the rearrangement of all the ethers takes place by a dissociation-recombination mechanism with the formation of the fluorenone-migrating group carbanion pair as intermediate.The migratory aptitude increases in the order methyl benzyl allyl.The orders of effectiveness were established for the bases, phase transfer catalysts, and solvent in the Wittig rearrangement.
