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(6-Benzoyl-3,4-dimethylcyclohex-3-enyl)(phenyl)methanone is a complex organic compound with the molecular formula C20H20O2. It is a derivative of cyclohexenone, featuring a benzoyl group at the 6-position and a phenyl group attached to the 3-carbon. This molecule is characterized by its aromatic and aliphatic components, which contribute to its unique chemical properties. It is a white crystalline solid and is often used in the synthesis of various pharmaceuticals and chemical intermediates due to its reactive ketone and benzene rings. The compound's structure allows for a range of chemical reactions, including nucleophilic addition, oxidation, and reduction, making it a versatile building block in organic chemistry.

975-70-2

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975-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 975-70-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 975-70:
(5*9)+(4*7)+(3*5)+(2*7)+(1*0)=102
102 % 10 = 2
So 975-70-2 is a valid CAS Registry Number.

975-70-2Relevant articles and documents

1,3-Diaryl-4,5,6,7-tetrahydro-2H-isoindole derivatives: A new series of potent and selective COX-2 inhibitors in which a sulfonyl group is not a structural requisite

Portevin,Tordjman,Pastoureau,Bonnet,De Nanteuil

, p. 4582 - 4593 (2007/10/03)

Novel tetrahydro-2H-isoindoles have been prepared and evaluated as inhibitors of the COX-2 isoenzyme. A 1,3-diaryl substitution on the central polycyclic ring system and absence of a sulfonyl moiety are the two structural features of this chemical series.

Etude de la photoisomerisation du dibenzoyl-4,5 dimethyl-1,2 cyclohexene trans

Vulpian, Regine,Bouteiller, Jean-Claude,Lauricella, Robert,Aycard, Jean-Pierre

, p. 842 - 844 (2007/10/02)

Irradiation (λ=300 nm) of trans 4,5-dibenzoyl 1,2-dimethyl cyclohexene A in a liquid phase affords two isomers of A; the 5t,6c-dibenzoyl 2,3r-dimethyl cyclohexene 1 and 4c,5t-dibenzoyl 2r-methyl 1-methylene cyclohexane 2 which were identified by analysis

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