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35050-24-9

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35050-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35050-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35050-24:
(7*3)+(6*5)+(5*0)+(4*5)+(3*0)+(2*2)+(1*4)=79
79 % 10 = 9
So 35050-24-9 is a valid CAS Registry Number.

35050-24-9Relevant academic research and scientific papers

C- ARYL GLYCOSID DERIVATIVES, PHARMACEUTICAL COMPOSITION, PREPARATION PROCESS AND USES THEREOF

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Paragraph 0096; 0161; 0162, (2017/04/19)

This invention relates to a kind of C-aryl glycoside derivatives, its pharmaceutical compositions, preparation methods, and uses thereof. The preparation method comprises: method 1: in a solvent, deprotecting the acetyl protecting groups of compound 1-f in the presence of a base; method 2: 1) compound 2-g reacts with via Mitsunobu reaction; 2) deprotecting the acetyl protecting groups of compound 2-f obtained from step 1; method 3: 1) compound 2-g reacts with via nucleophilic substitution reaction; 2) deprotecting the acetyl protecting groups of compound 3-f obtained from step 1. The pharmaceutical composition comprises a kind of C-aryl glycoside derivatives; it's pharmaceutically acceptable salts and/or prodrugs thereof and excipient thereof. This invention further relates to a kind of C-aryl glycoside derivatives, it's pharmaceutically acceptable salts or pharmaceutical compositions thereof for the use in preparation of a SGLT inhibitor. The C-aryl glycoside derivatives of this invention provides a new direction for the study of SGLT inhibitors.

Stereoselective synthesis of benzannulated spiroketals: Influence of the aromatic ring on reactivity and conformation

Liu, Guodong,Wurst, Jacqueline M.,Tan, Derek S.

supporting information; experimental part, p. 3670 - 3673 (2011/03/18)

Image Presented A systematic stereocontrolled synthesis of benzannulated spiroketals has been developed, using kinetic spirocyclization reactions of glycal epoxides, leading to a new AcOH-induced cyclization and valuable insights into the reactivity and c

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