519-56-2 Usage
General Description
Phenanthro[4,5-bcd]furan-3-ol is a chemical compound that belongs to the class of furan derivatives, which are organic compounds containing a five-membered ring consisting of four carbon atoms and one oxygen atom. This particular compound contains a phenanthrene skeleton, which is a polycyclic aromatic hydrocarbon composed of three fused benzene rings. The presence of the furan moiety in phenanthro[4,5-bcd]furan-3-ol gives it unique chemical and physical properties, making it potentially useful in various applications such as in organic synthesis, medicinal chemistry, and material science. Additionally, the hydroxyl group at position three of the furan ring makes it a potentially useful building block for the synthesis of more complex molecules. Phenanthro[4,5-bcd]furan-3-ol may have potential applications in drug development and materials chemistry due to its unique structure and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 519-56-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 519-56:
(5*5)+(4*1)+(3*9)+(2*5)+(1*6)=72
72 % 10 = 2
So 519-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H8O2/c15-10-7-6-9-5-4-8-2-1-3-11-12(8)13(9)14(10)16-11/h1-7,15H
519-56-2Relevant articles and documents
On Phenanthrene-4,5-quinones: a Synthesis of Morphenol
Hewgill, Frank R.,Stewart, Jeffery M.
, p. 1419 - 1420 (1984)
1,3,6,8-Tetra-t-butylphenanthrene-4,5-quinone (10) has been prepared as a short-lived species in solution, and rapidly rearranges to a dienone (12) which on debutylation yields morphenol (14): the corresponding 9,10-dihydroquinone (6) crystallises as its oxepine valence isomer (7).
Phenanthrene-4,5-quinones: a Synthesis of Morphenol
Hewgill, Frank R.,Stewart, Jeffery M.
, p. 1305 - 1312 (2007/10/02)
Oxidation of 1,3,6,8-tetra-t-butil-9,10-dihydrophenanthrene-4,5-diol (8), gave the corresponding 4,5-quinone (9), isolated as its oxepine valence isomer (19).Oxidation of 1,3,6,8-tetra-t-butilphenanthrene-4,5-diol (3) gave an even less stable quinone (4) which rearranged via its arene oxide valence isomer (26) to an enone (22).Acid catalysed debutylation of this produced morphenol (24).The annelated analogue (27) of the phenanthrenequinone (4) showed no tendency to rearrange.