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1,2,3,6-Tetra-O-benzoyl-α-D-mannopyranose is a synthetic carbohydrate derivative that features a D-mannopyranose core with four benzoyl groups attached to its hydroxyl groups. 1,2,3,6-Tetra-O-benzoyl-a-D-mannopyranose is characterized by its potential reactivity and structural properties, which make it a valuable intermediate in organic synthesis and carbohydrate chemistry.

56994-11-7

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56994-11-7 Usage

Uses

Used in Organic Synthesis:
1,2,3,6-Tetra-O-benzoyl-α-D-mannopyranose is used as a synthetic intermediate for the preparation of various complex organic molecules and compounds. Its benzoyl-protected hydroxyl groups provide a versatile platform for further chemical modifications and functionalization, facilitating the synthesis of target molecules with desired properties.
Used in Carbohydrate Chemistry:
In the field of carbohydrate chemistry, 1,2,3,6-Tetra-O-benzoyl-α-D-mannopyranose serves as a key building block for the construction of oligosaccharides, glycoconjugates, and other carbohydrate-based structures. Its protected hydroxyl groups allow for selective reactions and controlled synthesis, enabling the creation of complex carbohydrate architectures with potential applications in various industries.
Used in Pharmaceutical Industry:
1,2,3,6-Tetra-O-benzoyl-α-D-mannopyranose is used as a precursor in the development of glyco-based pharmaceuticals. Its ability to form complex carbohydrate structures makes it a valuable component in the synthesis of potential drug candidates targeting carbohydrate-binding proteins and receptors, which are implicated in various diseases and biological processes.
Used in Material Science:
In material science, 1,2,3,6-Tetra-O-benzoyl-α-D-mannopyranose can be utilized in the design and synthesis of carbohydrate-based materials, such as polymers, coatings, and films. These materials can exhibit unique properties, such as biocompatibility, biodegradability, and specific recognition capabilities, making them suitable for applications in areas like drug delivery, tissue engineering, and sensors.
Used in Food Industry:
1,2,3,6-Tetra-O-benzoyl-α-D-mannopyranose can be employed in the food industry as a component in the development of novel food additives, flavor enhancers, or sweeteners. Its ability to form complex carbohydrate structures may contribute to the creation of new taste profiles or improve the stability and shelf life of food products.

Check Digit Verification of cas no

The CAS Registry Mumber 56994-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,9 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56994-11:
(7*5)+(6*6)+(5*9)+(4*9)+(3*4)+(2*1)+(1*1)=167
167 % 10 = 7
So 56994-11-7 is a valid CAS Registry Number.

56994-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,6-Tetra-O-benzoyl-α-D-mannose

1.2 Other means of identification

Product number -
Other names [(3R,4S,6R)-4,5,6-tribenzoyloxy-3-hydroxyoxan-2-yl]methyl benzoate

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:56994-11-7 SDS

56994-11-7Relevant academic research and scientific papers

Parasite glycoconjugates. Part 4. Chemical synthesis of disaccharide and phosphorylated oligosaccharide fragments of Leishmania donovani antigenic lipophosphoglycan

Nikolaev, Andrey V.,Rutherford, Trevor J.,Ferguson, Michael A. J.,Brimacombe, John S.

, p. 1977 - 1988 (2007/10/02)

The disaccharide 1, tetraglycosyl monophosphate 2, hexaglycosyl diphosphate 3 and octaglycosyl triphosphate 4, which are fragments of the phosphoglycan portion of Leishmania donovani lipophosphoglycan, have been synthesized.Elongation of the chain was performed using the suitably protected glycobiosyl hydrogenphosphonate derivatives 5 and 6 for the successive introduction of glycobiosyl phosphate units.

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