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51019-55-7

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51019-55-7 Usage

Uses

Cyclohexyl(phenyl)acetic Acid can be used as chiral antichloinergic drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 51019-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,1 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51019-55:
(7*5)+(6*1)+(5*0)+(4*1)+(3*9)+(2*5)+(1*5)=87
87 % 10 = 7
So 51019-55-7 is a valid CAS Registry Number.

51019-55-7Relevant articles and documents

Clicked AC regioisomer cationic cyclodextrins for enantioseparation

Zhou, Jie,Liu, Yun,Lu, Yingying,Tang, Jian,Tang, Weihua

, p. 54512 - 54516 (2015/02/05)

Novel AC regioisomer cationic cyclodextrins have been successfully prepared with azide/alkyne click chemistry. The clicked CDs were explored for the enantioseparation of acidic racemates in capillary electrophoresis.

Iodide-catalyzed reductions: Development of a synthesis of phenylacetic acids

Milne, Jacqueline E.,Storz, Thomas,Colyer, John T.,Thiel, Oliver R.,Dilmeghani Seran, Mina,Larsen, Robert D.,Murry, Jerry A.

experimental part, p. 9519 - 9524 (2012/01/06)

A new convenient and scalable synthesis of phenylacetic acids has been developed via the iodide catalyzed reduction of mandelic acids. The procedure relies on in situ generation of hydroiodic acid from catalytic sodium iodide, employing phosphorus acid as the stoichiometric reductant.

Regioselective alkylation of lithium dienediolates of α,β- unsaturated carboxylic acids

Brun, Eva M.,Gil, Salvador,Mestres, Ramón,Parra, Margarita

, p. 1160 - 1165 (2007/10/03)

Lithium carboxylic acids dienediolates are regioselectively alkylated at the α-carbon by reaction with tosylates derived from both primary and secondary alcohols. Both regio- and diastereoselectivity are improved when compared with those obtained in the c

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