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18311-26-7

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18311-26-7 Usage

General Description

METHYL-6-O-TRIPHENYLMETHYL-ALPHA-D-GLUCOPYRANOSIDE is a chemical compound that is a derivative of glucose. It is a methylated alpha-D-glucopyranoside with a triphenylmethyl group attached to the sixth carbon of the glucose ring. METHYL-6-O-TRIPHENYLMETHYL-ALPHA-D-GLUCOPYRANOSIDE has various uses in organic synthesis and as a chemical reagent in laboratory experiments. It is often used as a protecting group for the hydroxyl groups on glucose molecules, as well as in the synthesis of complex carbohydrates and other bioactive compounds. Additionally, it can serve as a useful tool in studying carbohydrate-protein interactions and other biochemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 18311-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18311-26:
(7*1)+(6*8)+(5*3)+(4*1)+(3*1)+(2*2)+(1*6)=87
87 % 10 = 7
So 18311-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C26H28O6/c1-30-25-24(29)23(28)22(27)21(32-25)17-31-26(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20/h2-16,21-25,27-29H,17H2,1H3

18311-26-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-6-(trityloxymethyl)oxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names Methyl 6-O-tritylhexopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18311-26-7 SDS

18311-26-7Relevant articles and documents

Sugar derivatives as new 6-phosphogluconate dehydrogenase inhibitors selective for the parasite Trypanosoma brucei

Pasti, Claudia,Rinaldi, Eliana,Cervellati, Carlo,Dallocchio, Franco,Hardre, Renaud,Salmon, Laurent,Hanau, Stefania

, p. 1207 - 1214 (2003)

Sugar derivatives mimicking compounds which take part in the catalysed reaction have been assayed as alternative substrates and/or competitive inhibitors of 6-phosphogluconate dehydrogenase from Trypanosoma brucei and sheep liver. Phosphonate analogues ha

Ring-opening polymerization of lactones using binaphthyl-diyl hydrogen phosphate as organocatalyst and resulting monosaccharide functionalization of polylactones

Miao, Yong,Phuphuak, Yupin,Rousseau, Cyril,Bousquet, Till,Mortreux, Andre,Chirachanchai, Suwabun,Zinck, Philippe

, p. 2279 - 2287 (2013)

Binaphthyl-diyl hydrogen phosphate has been assessed for the first time as a catalyst for the ring-opening polymerization of ε-caprolactone (CL) and δ-valerolactone (VL). In the presence of benzyl alcohol as coinitiator at 40-60 °C, the polymerization is

Peptide-Coated Platinum Nanoparticles with Selective Toxicity against Liver Cancer Cells

Shoshan, Michal S.,Vonderach, Thomas,Hattendorf, Bodo,Wennemers, Helma

, p. 4901 - 4905 (2019)

Peptide-stabilized platinum nanoparticles (PtNPs) were developed that have significantly greater toxicity against hepatic cancer cells (HepG2) than against other cancer cells and non-cancerous liver cells. The peptide H-Lys-Pro-Gly-dLys-NH2 was identified by a combinatorial screening and further optimized to enable the formation of water-soluble, monodisperse PtNPs with average diameters of 2.5 nm that are stable for years. In comparison to cisplatin, the peptide-coated PtNPs are not only more toxic against hepatic cancer cells but have a significantly higher tumor cell selectivity. Cell viability and uptake studies revealed that high cellular uptake and an oxidative environment are key for the selective cytotoxicity of the peptide-coated PtNPs.

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Luckett,Smith

, p. 1506,1510 (1940)

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Chemoenzymatic synthesis of 3-deoxy-3-fluoro-l-fucose and its enzymatic incorporation into glycoconjugates

Valverde, Pablo,Vendeville, Jean-Baptiste,Hollingsworth, Kristian,Mattey, Ashley P.,Keenan, Tessa,Chidwick, Harriet,Ledru, Helene,Huonnic, Kler,Huang, Kun,Light, Mark E.,Turner, Nicholas,Jiménez-Barbero, Jesús,Galan, M. Carmen,Fascione, Martin A.,Flitsch, Sabine,Turnbull, W. Bruce,Linclau, Bruno

supporting information, p. 6408 - 6411 (2020/06/21)

The first synthesis of 3-deoxy-3-fluoro-l-fucose is presented, which employs ad- tol-sugar translation strategy, and involves an enzymatic oxidation of 3-deoxy-3-fluoro-l-fucitol. Enzymatic activation (FKP) and glycosylation using an α-1,2 and an α-1,3 fu

Chemical synthesis and preliminary biological evaluation of C-6-O-methyl-1-deoxynojirimycin as a potent α-glucosidase inhibitor

Wang, Lin,Liang, Tingting,Fang, Zhijie

, p. 36 - 49 (2019/12/24)

A facile and efficient synthesis of 6-O-methyl-1-deoxynojirimycin 4 from commercially available methyl α-D-glucopyranoside in 10 steps and 25% overall yield was reported. The synthetic strategy was based on the regioselective protection/deprotection at 6-

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