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Methyl-2,3,4-tri-O-methyl-α-D-xylopyranoside is a complex organic compound with the chemical formula C10H20O5. It is a derivative of α-D-xylopyranose, a monosaccharide sugar, where three hydroxyl groups at the 2nd, 3rd, and 4th carbon positions are replaced by methoxy groups. This modification results in a stable, non-reducing sugar that is commonly used in organic synthesis and as a protecting group in carbohydrate chemistry. The compound is also known for its potential applications in the pharmaceutical industry, particularly in the development of drugs targeting carbohydrate-binding proteins. Its structure provides a valuable tool for studying the interactions between sugars and proteins, which is crucial for understanding various biological processes and diseases.

7381-06-8

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7381-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7381-06-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7381-06:
(6*7)+(5*3)+(4*8)+(3*1)+(2*0)+(1*6)=98
98 % 10 = 8
So 7381-06-8 is a valid CAS Registry Number.

7381-06-8Downstream Products

7381-06-8Relevant academic research and scientific papers

PESTICIDAL COMPOSITIONS

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Page/Page column 7, (2010/08/18)

The invention disclosed in this document is related to the field of pesticides and their use in controlling pests. A compound having the following structure is disclosed.

PESTICIDAL COMPOSITIONS

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Page/Page column 18; 45, (2009/09/05)

The invention disclosed in this document is related to the field of pesticides and their use in controlling pests. A compound having the following structure is disclosed.

Peralkylation of Saccharides under Aqueous Conditions

Wang, Hui,Sun, Lihong,Glazebnik, Serge,Zhao, Kang

, p. 2953 - 2956 (2007/10/02)

Treatment of saccharides with sodium hydroxide and alkyl halides in aqueous dimethyl sulfoxide solution offers a very efficient method for the complete alkylation of saccharides in high yields.

THE STEROIDAL GLYCOSIDES OF THE FLOWERS OF YUCCA GLORIOSA

Nakano, Kimiko,Matsuda, Emi,Tsurumi, Kaori,Yamasaki, Tokushi,Murakami, Kotaro,et al.

, p. 3235 - 3240 (2007/10/02)

Four steroidal compounds were isolated from the fresh flowers of Yucca gloriosa and their structures were elucidated as tigogenin 3-O-β-D-xylopyranosyl-β-lycotetraoside, gitogenin 3-O-β-D-xylopyranosyl-β-lycotetraoside, gitogenin 3-O-α-rhamnopyranosyl-β-lycotetroside and proto-type of gitogenin 3-O-β-D-xylopyranosyl-β-lycotetraoside, on the basis of physical and chemical investigation.Key Word Index - Yucca gloriosa; Liliaceae; tigogenin glycoside; gitogenin glycosides; furostanol glycoside.

Entada Saponins (ES) II and IV from the Bark of Entada phaseoloides

Okada, Yoshihito,Shibata, Shoji,Javellana, Ana M. J.,Kamo, Osamu

, p. 1264 - 1269 (2007/10/02)

The structures of entada saponins II and IV, isolated from the bark of Entada phaseoloides (L.) Merrill (Leguminosae), were elucidated as 3-O-2)-α-L-arabinopyranosyl-(1->6)>4)>-2-acetamido-2-deoxy-β-D-glucopyranosyl-28-O-3)-β-D-xylopyranosyl(1->2)>4)>-6-O-((6R)-6-hydroxy-2,6-dimethyl-(2E)-2,7-octadienoyl)-β-D-glucopyranosyl olenolic acid (1) and entagenic acid (3).Keywords - Entada phaseoloides; Leguminosae; triterpene saponin; 13C-NMR chemical shift; entada saponin II; entada saponin IV

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