logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Tetrahydropyrans  > 2,3,4,6-Tetra-o-acetyl-a-d-mannopyranosyl trichloroacetimidate

AB53526

121238-27-5 | 2,3,4,6-Tetra-o-acetyl-a-d-mannopyranosyl trichloroacetimidate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $113.00 $79.00 -   +
250mg 95% in stock $206.00 $144.00 -   +
1g 95% in stock $465.00 $325.00 -   +
5g 95% in stock $1,323.00 $926.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Request Bulk Quote
Description
Catalog Number: AB53526
Chemical Name: 2,3,4,6-Tetra-o-acetyl-a-d-mannopyranosyl trichloroacetimidate
CAS Number: 121238-27-5
Molecular Formula: C16H20Cl3NO10
Molecular Weight: 492.6897
MDL Number: MFCD04039685
SMILES: CC(=O)OC[C@H]1O[C@H](OC(=N)C(Cl)(Cl)Cl)[C@H]([C@H]([C@@H]1OC(=O)C)OC(=O)C)OC(=O)C

 

Upstream Synthesis Route 
  • The 2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl trichloroacetimidate is a valuable reagent commonly employed in chemical synthesis for the purpose of glycosylation reactions. It serves as a versatile building block in the assembly of complex carbohydrates and glycoconjugates. By selectively activating the hydroxyl groups of mannose, this compound facilitates the controlled formation of glycosidic bonds, allowing for the precise tailoring of carbohydrate structures. Its trichloroacetimidate moiety acts as an efficient leaving group, promoting high regioselectivity and yielding reliable outcomes in the synthesis of diverse glycoconjugates. Additionally, the acetyl groups provide protection to the mannose unit during synthetic manipulations, ensuring the stability and integrity of the molecule throughout the chemical process. Through strategic utilization of 2,3,4,6-Tetra-O-acetyl-α-D-mannopyranosyl trichloroacetimidate in chemical synthesis, researchers can access a powerful tool for the controlled construction of complex carbohydrates with defined structures and functions.
FEATURED PRODUCTS