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1123095-73-7

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1123095-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1123095-73-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,3,0,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1123095-73:
(9*1)+(8*1)+(7*2)+(6*3)+(5*0)+(4*9)+(3*5)+(2*7)+(1*3)=117
117 % 10 = 7
So 1123095-73-7 is a valid CAS Registry Number.

1123095-73-7Downstream Products

1123095-73-7Relevant academic research and scientific papers

Total synthesis of valerenic acid, a potent gabaa receptor modulator

Ramharter, Juergen,Mulzer, Johann

, p. 1151 - 1153 (2009)

The first total synthesis of the sesquiterpenoid valerenic acid, a constituent of Valeriana officinalis, is described. The compound is a potent modulator of the GABAA receptor and may thus be useful in the treatment of various dysfunctions of the central

From planning to optimization: Total synthesis of valerenic acid and some bioactive derivatives

Ramharter, Juergen,Mulzer, Johann

, p. 2041 - 2053 (2012)

A detailed study of the total synthesis of valerenic acid, a well known GABAA receptor subtype modulator, is described. Both successful as well as unsuccessful attempts towards the synthesis of the title compound are presented, including four different strategies to synthesize one of the key intermediates. The first two strategies are based on epoxides provided from the chiral pool, whereas the last two approaches rest on stereocontrolled modifications of 2-cyclopentenone. The streamlined synthesis implements a new one-pot reaction, which combines the addition of a Grignard species with an acid-catalyzed isomerization of the intermediate allylic alcohol. Further highlights are a stereo- and regioselective hydroxy-directed Diels-Alder reaction, a hydroxy-directed hydrogenation, and a final Negishi coupling reaction. After optimization of our synthesis, the preparation of several easily available derivatives is also discussed. Amides obtained by functionalization of the carboxyl group are more than twice as active as valerenic acid. The development and optimization of four different approaches towards valerenic acid (1) are described. The shortest approach spans 10 steps and provides valerenic acid in 25 % overall yield by incorporating a new one-pot reaction, an extremely stereo- and regioselective metal-coordinated Diels-Alder reaction, a hydroxy-directed hydrogenation, and a final Negishi coupling reaction. Copyright

METHODS FOR MAKING VALERENIC ACID DERIVATIVES AND THEIR USE

-

Page/Page column 104, (2010/08/08)

The present invention is directed to compounds, intermediates and methods for making valerenic acid and its derivatives as well as the use of such compounds as GABAA receptor ligands.

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