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4-nitrophenyl ursodeoxycholate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91613-11-5

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91613-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91613-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,1 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91613-11:
(7*9)+(6*1)+(5*6)+(4*1)+(3*3)+(2*1)+(1*1)=115
115 % 10 = 5
So 91613-11-5 is a valid CAS Registry Number.

91613-11-5Downstream Products

91613-11-5Relevant academic research and scientific papers

Preparing method for tauro ursodesoxy cholic acid

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Paragraph 0040; 0041; 0042, (2016/10/09)

The invention discloses a preparing method for tauro ursodesoxy cholic acid. The method comprises the following steps that firstly, ursodesoxycholic acid and a phenolic compound are added into a chloralkane organic solvent at the room temperature, the temperature is lowered to 10-20 DEG C, a condensing agent is added, thorough reaction is carried out under the temperature of 5-45 DEG C in a heat preservation mode after dripping is completed, filter liquor is concentrated after filtering to obtain a crude product, and the crude product is recrystallized to obtain a ursodesoxycholic acid phenolic ester refined product; secondly, taurine salt and a crown ether complexing agent are added into water to be dissolved, a taurine salt crown ether complex is obtained after concentration, the ursodesoxycholic acid phenolic ester refined product and the taurine salt crown ether complex are added into an organic solvent to be reacted, acid is added after thorough reaction and stirred, solids are separated out and filtered, a filter cake is dissolved in water, stirred and subjected to crystallization, and tauro ursodesoxy cholic acid is obtained. The synthetic method is low in cost, operation is simple and controllable, the product is high in yield and purity, meanwhile, the isomer impurity taurochenodeoxycholic acid of tauro ursodesoxy cholic acid can be well controlled, and the preparing method is suitable for industrial production.

Preparation of New Haptens for Use in Immunoassay of Glycine-Conjugated Bile Acids

Miyairi, Shinichi,Shioya, Hiroaki,Ebihara, Mitsutaka,Hosoda, Hiroshi,Nambara, Toshio

, p. 1891 - 1897 (2007/10/02)

The N-succinimidyl esters of various glycine-conjugated bile acid 3-hemisuccinates and 3-hemiglutarates have been prepared for use in immunoassay.Unconjugated bile acids were condensed with p-nitrophenol to form the activated esters.Subsequent reaction wi

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