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2-methoxycarbonylphenyl β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98284-66-3

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98284-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98284-66-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,8 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 98284-66:
(7*9)+(6*8)+(5*2)+(4*8)+(3*4)+(2*6)+(1*6)=183
183 % 10 = 3
So 98284-66-3 is a valid CAS Registry Number.

98284-66-3Downstream Products

98284-66-3Relevant academic research and scientific papers

PHENOL GLYCOSIDES AND THEIR USE IN THE TREATMENT OF UROLITHIASIS

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Page/Page column 26; 27; 32; 33, (2017/01/26)

The present invention relates to novel derivatives of polyphenol glycoside or polyalcohols of formula (1), wherein R1, R2, R3 is selected from the group consisting of H, OH, C(O)R4, C(0) OR4, 0 (Gly H3)n, wherein n = 0 1, 2, 3, and R4 is selected from the group consisting of H, alkyl, and Gly is a mono- or disaccharide residue. The present invention also relates to novel derivatives of glycoside polyphenols or polyalcohols, as pharmaceutical composition comprising a novel polyphenol glycoside or polyalcohols and the use of novel polyphenol glycoside or polyalcohols for the treatment of urolithiasis.

Synthesis and anti-nociceptive and anti-inflammatory effects of gaultherin and its analogs

Wang, Chao,Zhang, Tian-Tai,Du, Guan-Hua,Zhang, Dong-Ming

scheme or table, p. 817 - 825 (2011/10/02)

The synthesis of gaultherin (1) and its analogs was carried out to provide 11 glycosides under phase-transfer catalytic conditions. The activities of all synthesized compounds were evaluated by nitric oxide production inhibitory assay in vitro. Methyl 2-O-(4-O-β- d-galactopyranosyl)- β- d-glucopyranosylbenzoate (5f) showed significantly anti-nociceptive and anti-inflammatory effects by the evaluation in vivo. Structure-activity relationships within these compounds were discussed.

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