33059-87-9

Usage

Chemical class

Acetylhexopyranoses
1,3,4,6-tetra-O-acetyl-2-{[(2-chloroethyl)carbamoyl]amino}-2-deoxyhexopyranose belongs to a group of hexopyranoses with acetyl groups attached.

Derivative of

2-deoxyhexopyranose
It is derived from 2-deoxyhexopyranose, a sugar molecule without an oxygen atom at the second carbon.

Acetyl groups

Attached to positions 1, 3, 4, and 6
These groups are responsible for the compound's reactivity and solubility in organic solvents.

Carbamoyl amino group

Present in the molecule
This functional group contributes to the compound's reactivity and potential applications in medicinal chemistry.

Chloroethyl group

Also present in the molecule
The presence of this group can be used for further functionalization and modification of the compound.

Application in organic synthesis

Used for the modification of carbohydrates
The compound can be used to modify other carbohydrate molecules, expanding the range of possible structures and applications.

Application in medicinal chemistry

Precursor for the synthesis of complex molecules
It serves as a starting material for the synthesis of more complex molecules with potential therapeutic applications.

Study of carbohydrate-protein interactions

Valuable tool
The compound's structure allows for the investigation of how carbohydrates interact with proteins, which is important for understanding biological processes and developing new drugs.

Development of potential therapeutic agents

Contributes to this field
The compound's unique structure and reactivity make it a useful tool in the development of new therapeutic agents targeting carbohydrate-protein interactions.