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3-[5-benzyloxy-2,3-dihydro-2,2,4,6-tetramethylbenzo[b]furan-7-yl]propanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137418-50-9

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137418-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137418-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,1 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137418-50:
(8*1)+(7*3)+(6*7)+(5*4)+(4*1)+(3*8)+(2*5)+(1*0)=129
129 % 10 = 9
So 137418-50-9 is a valid CAS Registry Number.

137418-50-9Upstream product

137418-50-9Relevant academic research and scientific papers

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 (1994)

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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