3615-47-2

Basic information

• Product Name: 2-O,3-O,4-O,6-O-Tetramethyl-D-glucose
• Synonyms: 2-O,3-O,4-O,6-O-Tetramethyl-D-glucose
• CAS NO: 3615-47-2
• Molecular Formula: C₁₀H₂₀O₆
• Molecular Weight: 236.26
• Mol File: 3615-47-2.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-O,3-O,4-O,6-O-Tetramethyl-D-glucose(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O,3-O,4-O,6-O-Tetramethyl-D-glucose(3615-47-2)
• EPA Substance Registry System: 2-O,3-O,4-O,6-O-Tetramethyl-D-glucose(3615-47-2)

Safety Data

• Hazardous Substances Data: 3615-47-2(Hazardous Substances Data)

Upstream product

• 9004-54-0 dextran 
• 2491-17-0 N-cyclohexyl-N'-β-(4-methylmorpholinium)ethylcarbodiimide p-toluenesulfonate 
• 108888-12-6 C₄₂H₇₀O₉ 
• 77-78-1 dimethyl sulfate 
• 81562-07-4 p-nitrophenyl 4,6-O-benzylidene-3-O-D-galactopyranosyl-β-D-galactopyranoside 
• 74-88-4 methyl iodide 

Downstream Products

• 25018-29-5 2,3,4,6,2',3',4',6'-octa-O-methyl-α,α-trehalose 
• 74720-58-4 O-(2,4-di-O-methyl-D-erythrose)-(1<*>2)-3-O-methyl-D-glyceraldehyde 
• 74720-61-9 O-(2,4-di-O-methyl-D-erythrose)-(1<*>3)-2,4-di-O-methyl-D-erythronic acid 
• 34338-82-4 methyl 2,3,5-tri-O-methyl-D-arabinoside 
• 74720-60-8 2,3,5-tri-O-methyl-D-arabinonolactone 
• 74720-59-5 1-O-formyl-2,3,5-tri-O-methyl-D-arabinose methyl hemiacetal 
• 35510-38-4 2,3,4,6-tetra-O-methyl-D-glucono-1,5-lactone 
• 15075-09-9 2.3.4.6-Tetra-O-methyl-D-mannose 
• 67-56-1 methanol 
• 64-18-6 formic acid 
• 15719-64-9 methylammonium carbonate 
• 20869-29-8 O²,O³,O⁵,O⁶-tetramethyl-D-galactonic acid-lactone 
• 59-23-4 D-Galactose 
• 25018-29-5 bis-(tetra-O-methyl-ξ-D-idopyranosyl)-ether 

Relevant articles and documents

A SPIROSTANOL GLYCOSIDE FROM AGAVE CANTALA

A new steroidal saponin has been isolated from the ethanolic extract of the roots of Agave cantala and shown to be 3-O--6-O--(25R)-5α-22α-O-spirostan-3β,6α-diol.Key Word Index - Agave cantala; Agavaceae; saponins; spirostanol glycoside; 3-O--6-O--(25R)-5α-22α-O-spirostan-3β,6α-diol.

Antibacterial Activity of a New Flavone Glycoside from the Stems of Holmskioldia sanguinea Retz.

A new flavone glycoside was isolated from ethanolic extract of stem parts of Holmskioldia sanguinea Retz. Its structure was characterized as 3,4′-dihydroxy-5,7-dimethoxyflavone-3-O-β-D-galactopyranosyl(1→4)-O-β-D-arabinopyranosyl-4′-O-α-L-rhamnopyranoside (1) by colour reactions, chemical degradation and spectroscopic analysis. Antibacterial activity of compound 1 was evaluated against various Gram positive and Gram negative bacteria showing a significant effects.

Allelopathic effect of triterpenoid saponins from the stems of lathyrus aphaca linn

Two new triterpenoid saponins have been isolated from the methanolic extract of the stems of the Lathyrus aphaca Linn. A new compound 1 has m.p. 295?297°C, m.f. C47H78O16, [M]+ m/z 898 was characterized as 3-O-[β-D-galactopyranosyl-(14)]-β-D-xylopyranosyl-3β,11α,28-trihydroxy-olean-12-ene-28-O-α-L-rhamnopyranoside and compound 2 has m. p. 289-291°C, m.f. C46H76O16, [M]+ m/z 884 was characterized as 3-O-[β-D-xylopyranosyl-(1→4)]-β-D-glucopyranosyl-(1→4) α-L-arabinofuranosyl 2α,3β,19α-trihydroxy-olean-12-ene by various color reactions, chemical degradations, and spectral analysis. From experimental findings, it was concluded that both compounds 1 and 2 have shown allelopathic effects on the growth of shoot length of the seeds of Zea mays (L.).