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(4S,4'S)-2,2'-Diphenyl-2,3,2',3'-tetrahydro-[4,4']bichromenyl-4,4'-diol is a complex organic compound with a molecular formula of C26H22O4. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of bichromanyl derivatives. (4S,4'S)-2,2'-Diphenyl-2,3,2',3'-tetrahydro-[4,4']bichromenyl-4,4'-diol is characterized by its unique structure, featuring two phenyl rings connected through a bichromanyl bridge, with hydroxyl groups at the 4 and 4' positions. It is synthesized through a series of chemical reactions and is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific stereochemistry and molecular properties.

508-08-7

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508-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 508-08-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 508-08:
(5*5)+(4*0)+(3*8)+(2*0)+(1*8)=57
57 % 10 = 7
So 508-08-7 is a valid CAS Registry Number.

508-08-7Downstream Products

508-08-7Relevant academic research and scientific papers

Photoreactions of Flavanones

Matsushima, Ryoka,Kishimoto, Tsuneo,Suzuki, Morio,Morioka, Motonobu,Mizuno, Hideo

, p. 2938 - 2942 (1980)

Parent and substituted flavanones undergo photochemical opening of the pyrone ring to give corresponding 2'-hydroxychalcones in benzene, acetonitrile etc., the yields varying from 0 to 70percent with substituents.The reaction is depressed by the addition of 1,3-pentadiene, nitrosobenzene, or acrylonitrile.On the other hand, flavanone and 4-chromanone undergo photoreduction in 2-propanol to give reductive coupling products and solvent adducts as isomeric mixtures. 7,8-Benzoflavanone does not undergo photoreduction in 2-propanol but the ring opening reaction instead.Mechanisms have been discussed in terms of the relative contribution of n,?* and ?,?* character in the lowest triplet states.

Specific Photoreactions of Flavanones Typical of n,?* and ?,?* Characters in Lowest Triplet States

Matsushima, Ryoka,Sakai, Katsuhisa

, p. 1217 - 1222 (2007/10/02)

On irradiation with u.v. light, flavanones undergo photochemical opening of the dihydropyranone ring (φ2 3 2, φ3, and γ with substituents are explicable in terms of relative contributions of n,?* and ?,?* character in lowest triplet states.

HYDRODIMERISATION ELECTROCHIMIQUE DE CETONES AROMATIQUES ENCOMBREES EN MILIEU APROTIQUE ET EN PRESENCE DE CHLORURE DE CHROME

Fournier, F.,Berthelot, J.,Pascal, Y. L.

, p. 339 - 347 (2007/10/02)

The electrochemical reduction of hindered aromatic ketones which are difficult to reduce alone, can be achieved in an aprotic medium (DMF) on a mercury pool cathode, in presence of Cr(III) chloride, at the reduction potential of the Cr(II)/Cr(0) system, but at a less negative potential than that of the ketone itself.There is a selective hydrodimerisation into an α-glycol, with total lack of polimerisation.With disymmetric ketones, the dl-diastereoisomers of the diols are produced.The effect of chromium is due either to the reduction of a Cr-ketone complex or to thereduction of the ketone by a film of colloidal chromium on the electrode surface.

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