3352-82-7 Usage
General Description
6-Hydroxy-1H-phenalen-1-one is a chemical compound also known as phenalene-1,2-dione. It belongs to the class of compounds known as phenalenones, which are a type of polycyclic aromatic hydrocarbons (PAHs). 6-HYDROXY-1H-PHENALEN-1-ONE has a molecular formula of C13H8O2 and a molecular weight of 196.2 g/mol. It is a yellowish solid at room temperature with a melting point of around 163-165°C. 6-Hydroxy-1H-phenalen-1-one is used in organic synthesis and chemical research as a reactant in various reactions and as a building block for the synthesis of more complex organic compounds. It also has potential applications in the field of materials science and can be used as a fluorescent probe in biological research. However, like other PAHs, it is important to handle this compound with care due to its potential health hazards.
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 articles and documents
Improved synthesis of natural isomeric naphthoxanthenones
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
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.
