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93554-97-3

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93554-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93554-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,5,5 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93554-97:
(7*9)+(6*3)+(5*5)+(4*5)+(3*4)+(2*9)+(1*7)=163
163 % 10 = 3
So 93554-97-3 is a valid CAS Registry Number.

93554-97-3Relevant articles and documents

Towards a rational design for resolving agents. Part V; Substituent effects in the resolution of ephedrine using a series of cyclic phosphoric acids

Haest, Albertus D. van der,Wynberg, Hans,Leusen, Frank, J. J.,Bruggink, Alle

, p. 230 - 235 (1993)

The effects of various aromatic substituents in both ephedrine and a cyclic phosphoric acid on the quality of resolution via diastereomeric salt formation are investigated.The diastereoselective synthesis of a novel series of chloro-substituted ephedrines

PYRAZOLE AMIDE DERIVATIVE

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Page/Page column 113; 114, (2015/09/28)

The present invention relates to a novel compound having a function of inhibiting RORγ activity. The present invention also relates to pharmaceutical composition comprising the compound, a use of the compound in treating or preventing autoimmune diseases, inflammatory diseases, metabolic diseases, or cancer diseases.

Preparation, characterization and catalytic properties of polyaniline-supported metal complexes

Choudary, Boyapati M.,Roy, Moumita,Roy, Sarabindu,Kantam, M. Lakshmi,Sreedhar, Bojja,Kumar, Karasala Vijay

, p. 1734 - 1742 (2007/10/03)

Polyaniline-supported Sc, In, Pd, Os and Re catalysts were prepared by using a simple protocol and the thus prepared catalysts were well characterized using FTIR, XPS, UV-Vis/DRS, TGA-DTA. All the catalysts were successfully employed in a wide range of organic transformations such as cyanation and allylation of carbonyl compound, Suzuki coupling of aryl halides and boronic acids, and, most importantly, in asymmetric dihydroxylation of olefins to afford optically active vicinal diols. All the catalysts were separated from the reaction mixture by simple filtration and reused with consistent activity for five cycles without noticeable leaching of metal from the support.

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