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8-Methoxydihydrocoumarin is a chemical compound belonging to the class of dihydrocoumarins, which are reduced forms of coumarins. It is characterized by the presence of a methoxy group (-OCH3) at the 8-position of the dihydrocoumarin structure. 8-methoxydihydrocoumarin is an organic molecule with potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties. The presence of the methoxy group can influence the compound's reactivity, solubility, and biological activity, making it a valuable intermediate in organic synthesis.

80515-75-9

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80515-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80515-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80515-75:
(7*8)+(6*0)+(5*5)+(4*1)+(3*5)+(2*7)+(1*5)=119
119 % 10 = 9
So 80515-75-9 is a valid CAS Registry Number.

80515-75-9Relevant academic research and scientific papers

Organocatalyst-Mediated Dynamic Kinetic Enantioselective Acylation of 2-Chromanols

Glazier, Daniel A.,Schroeder, John M.,Liu, Jitian,Tang, Weiping

supporting information, p. 4646 - 4649 (2018/11/10)

We recently developed a novel chiral catalyst-directed dynamic kinetic diastereoselective acylation of hemiacetals for the synthesis of carbohydrates. In this update, we describe a catalytic method for the dynamic kinetic enantioselective acylation of 2-c

New Syntheses of Coumarins

Panetta, Jill A.,Rapoport, Henry

, p. 946 - 950 (2007/10/02)

New, versatile coumarin syntheses have been developed which are based on the Claisen rearrangement of allylic or propargylic aryl ethers in which the allylic or propargylic α-carbon is further oxygenated.One proceeds by first ester exchange to the aryl dialkyl orthoacrylate which then thermally rearranges.Hydrolytic treatment gives the o-hydroxydihydrocinnamic acid from which the coumarin is obtained by ring closure and dehydrogenation.In parallel fashion, an orthopropiolate may be used, eliminating the dehydrogenation step.These processes have the adventage ofavoiding the drastic acid conditions and orientation limitations of previous coumarin syntheses.They have been applied to syntheses in good yields of coumarins obtainable by previous methods in very poor yield or not at all.

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