3352-82-7 Usage
Uses
Used in Organic Synthesis:
6-Hydroxy-1H-phenalen-1-one is used as a reactant in various organic synthesis reactions, contributing to the formation of more complex organic compounds.
Used in Chemical Research:
In the field of chemical research, 6-Hydroxy-1H-phenalen-1-one serves as a building block for the synthesis of intricate organic molecules, facilitating the development of novel chemical entities.
Used in Materials Science:
6-Hydroxy-1H-phenalen-1-one has potential applications in materials science, where it can be utilized to create new materials with unique properties.
Used as a Fluorescent Probe in Biological Research:
In biological research, 6-Hydroxy-1H-phenalen-1-one can be employed as a fluorescent probe, enabling the study of biological processes and interactions at the molecular level.
Caution:
As with other PAHs, 6-Hydroxy-1H-phenalen-1-one should be handled with care due to its potential health hazards. Proper safety measures and precautions are essential when working with 6-HYDROXY-1H-PHENALEN-1-ONE to minimize risks.
Check Digit Verification of cas no
The CAS Registry Mumber 3352-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3352-82:
(6*3)+(5*3)+(4*5)+(3*2)+(2*8)+(1*2)=77
77 % 10 = 7
So 3352-82-7 is a valid CAS Registry Number.
3352-82-7Relevant academic research and scientific papers
Barrera, Julian,Pati?o, Edwin,Otálvaro, Felipe
, (2020)
5-methoxy-1H-naphtho[2,1,8-mna]xanthen-1-one (1) and 5-methoxy-3H-naphtho[2,1,8-mna]xanthen-3-one (musafluorone 2), a pair of positional isomers isolated from Wachendorfia thyrsiflora and Musa acuminata, were synthesized in six steps in an overall yield o
Synthesis of [phenyl-13C6]lachnanthocarpone and other 13C-labelled phenylphenalenones
Otalvaro, Felipe,Quinones, Winston,Echeverri, Fernando,Schneider, Bernd
, p. 147 - 159 (2007/10/03)
[phenyl-13C6]Lachnanthocarpone ([phenyl- 13C6]2,6-dihydroxy-9-phenylphenalen-1-one), a hypothetical intermediate in the biosynthesis of various natural phenylphenalenones, was prepared in four steps using [U- s
PRODUCTS FROM PHOTOLYSIS OF PHENALENONE IN ALCOHOL MEDIA
Kuznetsova, N.A.,Kaliya, O.L.,Sergeeva, N.D.,Solodar, S.L.
, p. 348 - 351 (2007/10/02)
Secondary reactions with the addition of the alcohol radicals to the ketyl radical of the phenalenone were observed during the irradiation of phenalenone in alcohols.In the presence of oxygen hydroxyphenalenones are formed in addition to the α-hydroxyalkyl derivatives.The dimerization and disproportionation processes are ineffective in the ketyl radicals of phenalenone.
