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Home  > Chemistry  > Heterocyclic Building Blocks  > Tetrahydropyrans  > 1,3,4,6-Tetra-o-acetyl-2-amino-2-deoxy-beta-d-glucopyranose, HCl

AA01964

10034-20-5 | 1,3,4,6-Tetra-o-acetyl-2-amino-2-deoxy-beta-d-glucopyranose, HCl

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $16.00 $11.00 -   +
1g 95% in stock $19.00 $13.00 -   +
5g 95% in stock $57.00 $40.00 -   +
10g 95% in stock $75.00 $52.00 -   +
25g 95% in stock $179.00 $125.00 -   +
100g 95% in stock $628.00 $440.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA01964
Chemical Name: 1,3,4,6-Tetra-o-acetyl-2-amino-2-deoxy-beta-d-glucopyranose, HCl
CAS Number: 10034-20-5
Molecular Formula: C14H22ClNO9
Molecular Weight: 383.7788
MDL Number: MFCD01075204
SMILES: CC(=O)OC[C@H]1O[C@@H](OC(=O)C)[C@@H]([C@H]([C@@H]1OC(=O)C)OC(=O)C)N.Cl

 

Computed Properties
Complexity: 507  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 5  
Heavy Atom Count: 25  
Hydrogen Bond Acceptor Count: 10  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 9  

 

 

Upstream Synthesis Route
  • The compound (2S,3R,4R,5S,6R)-6-(Acetoxymethyl)-3-aminotetrahydro-2H-pyran-2,4,5-triyl triacetate hydrochloride plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing multiple functional groups makes it a valuable intermediate in the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and specialty chemicals. This compound can be used to introduce the aminotetrahydro-2H-pyran scaffold into various target molecules, allowing for the modification and fine-tuning of their properties. Additionally, the presence of multiple acetyl groups provides opportunities for further derivatization to tailor the compound for specific applications in drug discovery and materials science. Overall, the (2S,3R,4R,5S,6R)-6-(Acetoxymethyl)-3-aminotetrahydro-2H-pyran-2,4,5-triyl triacetate hydrochloride is a valuable tool in the hands of synthetic chemists for the construction of diverse and intricate molecular structures.
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