6736-97-6

Basic information

• Product Name: 2-O,3-O,4-O,5-O,6-O-Pentakis(trimethylsilyl)-D-glucose
• Synonyms: 2-O,3-O,4-O,5-O,6-O-Pentakis(trimethylsilyl)-D-glucose
• CAS NO: 6736-97-6
• Molecular Formula: C21H52O6Si5
• Molecular Weight: 541.06
• Mol File: 6736-97-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-O,3-O,4-O,5-O,6-O-Pentakis(trimethylsilyl)-D-glucose(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O,3-O,4-O,5-O,6-O-Pentakis(trimethylsilyl)-D-glucose(6736-97-6)
• EPA Substance Registry System: 2-O,3-O,4-O,5-O,6-O-Pentakis(trimethylsilyl)-D-glucose(6736-97-6)

Safety Data

• Hazardous Substances Data: 6736-97-6(Hazardous Substances Data)

Upstream product

• 10416-59-8 N,O-bis-(trimethylsilyl)-acetamide 
• 50-99-7 D-glucose 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 1176306-07-2 1-O-3,4-(dihydroxyphenyl)ethyl-β-D-apiofuranosyl-(1->2)-β-D-xylopyranosyl-(1->3)-4-O-caffeoyl-β-D-glucopyranoside 
• 18156-74-6 1-(Trimethylsilyl)imidazole 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 34272-03-2 propargyl β-D-glucopyranoside 
• 151168-60-4 prop-2-ynyl-α-D-glucopyranoside 

Relevant articles and documents

Further 2R-Benzylmalate derivatives from the undergrounds parts of Arundina graminifolia (Orchidaceae)

Nine new glucosyloxybenzyl 2R-benzylmalate derivatives, named arundinosides R–Z (1-9) were isolated from the underground parts of Arundina graminifolia. The structures of the new compounds were elucidated by in-depth spectroscopic data analysis including

Novel quercetin glucosides from Helminthostachys zeylanica root and acceleratory activity of melanin biosynthesis

Two novel quercetin glucosides, namely 4′-O-β-d-glucopyranosyl- quercetin-3-O-β-d-glucopyranosyl-(1→4)-β-d-glucopyranoside (compound 1) and 4′-O-β-d-glucopyranosyl-(1→2)-β-d- glucopyranosyl-quercetin-3-O-β-d-glucopyranosyl-(1→4) -β-d-glucopyranoside (compound 2), were isolated from Helminthostachys zeylanica root 50 % EtOH extract. Structural analysis of isolated compounds was achieved mainly by 600 MHz and 800 MHz NMR, UPLC-TOFMS and GC-MS. Of the two quercetin glucosides, compound 1 showed a high melanogenic acceleratory effect, 2.7 times higher than control, at 10 μM concentration in murine B16 melanoma cells, with no cytotoxic effect.

Triterpenoid saponins from Gynostemma pentaphyllum

Four new dammarane-type triterpene saponins, 1-4, were isolated from the aerial parts of Gynostemma pentaphyllum (Thunb.) Makino. Their structural elucidations were accomplished mainly on the basis of spectroscopic methods, such as IR, HR-TOF-MS, and NMR. Compounds 1-4 showed moderate cytotoxic activities against cancer cell lines HL-60, Colon205, and Du145 in vitro.