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Methyl-2,3,4,6-tetra-O-methyl-D-glucopyranoside is a complex organic compound with the chemical formula C11H20O6. It is a derivative of D-glucose, a monosaccharide, where four hydroxyl groups are replaced by methyl groups, resulting in a tetra-O-methylated product. methyl-2,3,4,6-tetra-O-methyl-D-glucopyranoside is often used in organic synthesis and as a protecting group in carbohydrate chemistry, particularly in the synthesis of complex oligosaccharides and glycoconjugates. The methyl groups help to prevent unwanted reactions at the hydroxyl groups, allowing for selective modification of the remaining functional groups. Its structure provides a stable and less reactive intermediate, which is crucial for the controlled synthesis of more complex carbohydrate structures.

4117-96-8

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4117-96-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4117-96-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4117-96:
(6*4)+(5*1)+(4*1)+(3*7)+(2*9)+(1*6)=78
78 % 10 = 8
So 4117-96-8 is a valid CAS Registry Number.

4117-96-8Relevant academic research and scientific papers

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

Comparative Studies on the Constituents of a Parasitic Plant and Its Host. III. On the Constituents of Boschniakia rossica FEDTSCH, et FLEROV. (2)

Konishi, Tenji,Narumi, Yoko,Watanabe, Kazuaki,Kiyosawa, Shiu,Shoji, Junzo

, p. 4155 - 4161 (2007/10/02)

Two iridoid glucosides, namely boschnaloside (2), (+)-pinoresinol-β-D-glucopyranoside (3), a new oligosaccharide (=β-D-glucopyranosyl(1->4)-α-L-rhamnopyranosyl-(1->3)-D-(4-O-caffeoyl)-glucopyranose) (4), and a new phenylpropanoid glycoside named rossicaside A (5) have been isolated from Boschniakia rossica FEDTSCH, et FLEROV (Orobanchaceae) and their structures have been determined.Keywords--Boschniakia rossica; Orobanchaceae; boschnaloside; boschnaside; (+)-pinoresinol-β-D-glucoside; acetylated oligosaccharide; rossicaside A; phenylpropanoid glycoside

Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLV. Chemische Untersuchungen der Inhaltstoffe von Glaphyropteridopsis erubescens (Wall.) Copel.

Tanaka, Nobutoshi,Sada, Takuro,Murakami, Takao,Saiki, Yasuhisa,Chen, Chiu-Ming

, p. 490 - 496 (2007/10/02)

The fronds extracts of Glaphyropteridopsis erubescens (Wall.) Copel. contain besides the already known flavonol glycosides (afzelin and quercitrin) three new flavan-4-ol glycosides, eruberin A(I), B(II) and C(III), which belong to a new type of proanthocyanidin.By means of spectroscopic and chemical methods, the structures 5,7-dihydroxy-4'-methoxy-6,8-dimethyl-2'',4(S)-oxido-2(R)-flavan-5-β-D-glucopyranoside (I), 4(S),5,7-trihydroxy-4'-methoxy-6,8-dimethyl-2(R)-flavan-5,7-O-β-D-diglucopyranoside (II) and 5,7-dihydroxy-4(S),4'-dimethoxy-6,8-dimethyl-2(R)-flavan-5,7-O-β-D-diglucopyranoside (III) are proposed.Eruberin C(III) may be an artifact. Keywords - Glaphyropteridopsis erubescens; fern; Thelypteridaceae; chemotaxonomy; flavan-4-ol glycoside; structure; spectroscopic method; chemical reaction

STRUCTURAL INVESTIGATION OF Klebsiella K-TYPE 4 CAPSULAR POLYSACCHARIDE

Merrifield, Edwin H.,Stephen, Alistair M.

, p. 113 - 120 (2007/10/02)

The capsular polysaccharide from Klebsiella K4 contains the tetrasaccharide repeating-sequence 3)-α-D-Glcp-(12)-α-D-GlcpA-(13)-α-D-Manp-(13)-β-D-Glcp-(1.P.m.r. spectroscopy and the measurement of optical rotation were used to establish the anomeric linkages in the polysaccharide and in the oligosaccharides derived by partial hydrolysis.The repeating unit also contains one O-acetyl group.

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