22170-16-7 Usage
Description
O6-Benzyl-D-glucose is a chemical compound that consists of a D-glucose molecule with a benzyl group attached to the sixth carbon position. It is widely used in organic synthesis as a protecting group for the hydroxyl group of glucose, allowing for selective manipulation of other functional groups present in the molecule. This enables the synthesis of more complex compounds. O6-Benzyl-D-glucose is also utilized in the pharmaceutical industry for the production of various drugs and as a starting material for the synthesis of other important compounds. Furthermore, it has potential applications in the development of carbohydrate-based materials and as a probe for studying carbohydrate-protein interactions.
Uses
Used in Organic Synthesis:
O6-Benzyl-D-glucose is used as a protecting group for the hydroxyl group of glucose in organic synthesis for selective manipulation of other functional groups, enabling the synthesis of more complex compounds.
Used in Pharmaceutical Industry:
O6-Benzyl-D-glucose is used as a starting material for the production of various drugs and the synthesis of other important compounds in the pharmaceutical industry.
Used in Carbohydrate-based Materials Development:
O6-Benzyl-D-glucose is used as a component in the development of carbohydrate-based materials due to its unique structure and properties.
Used in Studying Carbohydrate-Protein Interactions:
O6-Benzyl-D-glucose is used as a probe for studying carbohydrate-protein interactions, providing insights into the biological roles and mechanisms of these interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 22170-16-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,7 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22170-16:
(7*2)+(6*2)+(5*1)+(4*7)+(3*0)+(2*1)+(1*6)=67
67 % 10 = 7
So 22170-16-7 is a valid CAS Registry Number.
22170-16-7Relevant articles and documents
A practical approach to regioselective O-benzylation of primary positions of polyols
Giordano, Maddalena,Iadonisi, Alfonso
, p. 1550 - 1552 (2013/03/14)
Exposure of saccharide polyols to a moderate excess of benzyl bromide and DIPEA at 90 °C results in the regioselective O-benzylation of primary positions in moderate to good yields. The reactions can be performed without inert atmosphere and provide synth
