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2-(acetylamino)-2-deoxy-6-O-tritylhexopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6959-53-1

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6959-53-1 Usage

Molecular Structure

A chemical compound consisting of a hexose ring with a trityl group attached to the 6th carbon and an acetylamino group attached to the 2nd carbon.

Derivative

It is a derivative of glucose.

Use as a protecting group

Used in organic chemistry as a protecting group for the hydroxyl group on the 6th carbon.

Trityl group

Provides protection for the hydroxyl group.

Acetylamino group

Serves as a temporary block for the 2nd carbon.

Applications

Commonly used in the synthesis and modification of carbohydrate molecules, as well as in the study of carbohydrate-protein interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 6959-53-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,5 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6959-53:
(6*6)+(5*9)+(4*5)+(3*9)+(2*5)+(1*3)=141
141 % 10 = 1
So 6959-53-1 is a valid CAS Registry Number.

6959-53-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (776521)  6-O-Trityl-N-acetyl-D-glucosamine  

  • 6959-53-1

  • 776521-500MG

  • 2,432.43CNY

  • Detail
  • Aldrich

  • (776521)  6-O-Trityl-N-acetyl-D-glucosamine  

  • 6959-53-1

  • 776521-2.5G

  • 6,505.20CNY

  • Detail

6959-53-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,4,5-trihydroxy-6-((trityloxy)methyl)tetrahydro-2H-pyran-3-yl)acetamide

1.2 Other means of identification

Product number -
Other names -

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:6959-53-1 SDS

6959-53-1Relevant academic research and scientific papers

Modelling, synthesis and biological evaluation of novel glucuronide-based probes of Vibrio cholerae sialidase

Mann, Maretta C.,Thomson, Robin J.,Dyason, Jeffrey C.,McAtamney, Sarah,Von Itzstein, Mark

, p. 1518 - 1537 (2006)

The development of sialidase inhibitors is an area of continuing interest due to their potential use as therapeutic agents to combat viral and bacterial infections. Herein, we report our studies involving the sialidase from the pathogen Vibrio cholerae, t

SHORT-CHAIN FATTY ACID HEXOSAMINE ANALOGS AND THEIR USE IN TISSUE ENGINEERING APPLICATIONS

-

Paragraph 0108, (2014/10/18)

A new class of molecules, C1-OH tributanoylated hexosamines, including, for example, Ga1NAc, G1cNAc and ManNAc, are demonstrated to increase cartilage-like tissue accumulation by IL- 1β-stimulated chondrocytes. Furthermore, all three molecules

Synthesis of five nona-β-(1→6)-d-glucosamines with various patterns of N-acetylation corresponding to the fragments of exopolysaccharide of Staphylococcus aureus

Yudina, Olga N.,Gening, Marina L.,Tsvetkov, Yury E.,Grachev, Alexey A.,Pier, Gerald B.,Nifantiev, Nikolay E.

experimental part, p. 905 - 913 (2011/06/20)

A series of five 3-acetamidopropyl β-glycosides of nona-β-(1→6)-glucosamines containing two N-acetylglucosamine residues separated by a different number of glucosamine units with free amino groups have been synthesized using a convergent blockwise approac

HYBRID SCFA-HYDROXYL-DERIVATIZED MONOSACCHARIDES, METHODS OF SYNTHESIS, AND METHODS OF TREATING DISORDERS

-

Page/Page column 50-51, (2009/07/03)

Described herein are fatty acid carbohydrate-hydroxyl-hybrid compounds and derivatives thereof, and methods of treating or preventing disease and disease symptoms using the compounds and compositions thereof.

An efficient approach to N-acetyl-D-glucosaminuronic acid-based sialylmimetics as potential sialidase inhibitors

Mann, Maretta C.,Thomson, Robin J.,Von Itzstein, Mark

, p. 5555 - 5558 (2007/10/03)

The synthesis of Neu5Ac2en mimetics as inhibitors of Vibrio cholerae sialidase is reported. A novel approach to the synthesis of β-glycosides of N-acetyl-d-glucosaminuronic acid, in six steps and good overall yield from N-acetyl-d-glucosamine, has been de

The reaction of partially protected aldoses with stabilized arsonium ylides: Synthesis of E acyclic unsaturated derivatives and C-glycosyl derivatives

Lievre, Catherine,Frechou, Catherine,Demailly, Gilles

, p. 1 - 15 (2007/10/03)

The reaction of partially protected aldoses with (carbomethoxymethyl)triphenylarsonium bromide and zinc in toluene gave E α,β-unsaturated acyclic esters. When intramolecular transesterification occurred, bicyclic 1,4-lactone derivatives were formed concurrently. Otherwise, using these non alcaline conditions, olefination did not favour the formation of C-glycosyl derivatives. On the other hand, when the reaction was performed with (carbomethoxymethylene)triphenylarsorane in toluene, followed by the addition of n-butyllithium, bicyclic derivatives were obtained rapidly in good yields. Moreover, when cyanomethyltriphenylarsonium bromide was used in place of (carbomethoxymethyl)triphenylarsonium bromide, the corresponding E aldooctenonitriles were produced in satisfactory yields.

FLUORINATED CARBOHYDRATES AS POTENTIAL PLASMA MEMBRANE MODIFIERS AND INHIBITORS. SYNTHESIS OF 2-ACETAMIDO-2,6-DIDEOXY-6-FLUORO-D-GALACTOSE

Sharma, Moheswar,Potti, Gopalan G.,Simmons, Onda D.,Korytnyk, Walter

, p. 41 - 52 (2007/10/02)

Reaction of benzyl 2-acetamido-3,4-di-O-benzyl-2-deoxy-6-O-mesyl-α-D-galactopyranoside with cesium fluoride gave benzyl 2-acetamido-3,6-anhydro-4-O-benzyl-2-deoxy-α-D-galactopyranoside instead of the desired 6-fluoro derivative.Acetonation of benzyl 2-ace

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