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1,4-Benzenediol, 3,5-dimethyl-2-(2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67883-66-3

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67883-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67883-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,8 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67883-66:
(7*6)+(6*7)+(5*8)+(4*8)+(3*3)+(2*6)+(1*6)=183
183 % 10 = 3
So 67883-66-3 is a valid CAS Registry Number.

67883-66-3Downstream Products

67883-66-3Relevant academic research and scientific papers

Bi(OTf)3-catalyzed allylation of quinones with allyltrimethylsilane

Yadav,Reddy,Swamy

, p. 4861 - 4864 (2007/10/03)

p-Quinones react smoothly with allyltrimethylsilane in the presence of 2 mol% of Bi(OTf)3 under mild reaction conditions to afford the corresponding allyl substituted benzene derivatives, p-allylquinols and allyl substituted 1,4-naphthoquinones in excellent yields with high regioselectivity. This method is very useful for the direct introduction of an allyl functionality onto a quinone moiety.

SYNTHESIS OF A NEW TYPE OF ANTIOXIDANT POSSESSING INHIBITORY ACTIVITY AGAINST HMG-CoA REDUCTASE

Matsumoto, Masakatsu,Watanabe, Nobuko,Mori, Eiko,Aoyama, Misao,Kusunoki, Jun,Yamaura, Tetsuaki

, p. 2589 - 2592 (2007/10/02)

The 6-hydroxychromans (4) and (6), and 5-hydroxy-2,3-dihydrobenzofurans (5) and (7) bearing a 4-hydroxypyran-2-one moiety were synthesized.All the compounds exhibited potent activity against lipid peroxidation.The chroman (4) possessed inhibitory activ

4-Hydroxytetrahydropyran-2-one derivatives

-

, (2008/06/13)

4-hydroxytetrahydropyran-2-one derivatives with general formula (I) are useful as cholesterol reducing agents as well as lipid reducing agents, serving as inhibitors of HMG-CoA reductase, and capable of inhibiting the biosynthesis of peroxidized lipids, and therefore effective for curing arteriosclerosis: STR1 wherein R1 represent hydrogen or a 2-tetrahydropyranyl group; R2 and R3 each represent hydrogen or an alkyl group having 1 to 6 carbon atoms; R4 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, an aryl group, an aralkyl group, an acyl group, an aroyl group or a substituted sulfonyl group; A represents --CH2 CH2 --, or --CH=CH--; and n is an integer of 1 or 2, and intermediates for synthesizing the 4-hydroxytetrahydropyran-2-one derivatives are disclosed.

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