2-(AcetylaMino)-2-deoxy-β-D-galactopyranosylaMine 3,4,6-Triacetate

Base Information

Chemical Name:2-(AcetylaMino)-2-deoxy-β-D-galactopyranosylaMine 3,4,6-Triacetate
CAS No.:39541-22-5
Molecular Formula:C₁₄H₂₂N₂O₈
Molecular Weight:346.337
Hs Code.:
Mol file:39541-22-5.mol

Synonyms:(2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-aminotetrahydro-2H-pyran-3,4-diyl diacetate

Suppliers and Price of 2-(AcetylaMino)-2-deoxy-β-D-galactopyranosylaMine 3,4,6-Triacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
2-(Acetylamino)-2-deoxy-β-D-galactopyranosylamine3,4,6-Triacetate
1g
$ 1190.00

TRC
2-(Acetylamino)-2-deoxy-β-D-galactopyranosylamine3,4,6-Triacetate
100mg
$ 150.00

Medical Isotopes, Inc.
2-(Acetylamino)-2-deoxy-β-D-galactopyranosylamine3,4,6-Triacetate
1 g
$ 2200.00

Total 5 raw suppliers

Chemical Property of 2-(AcetylaMino)-2-deoxy-β-D-galactopyranosylaMine 3,4,6-Triacetate

Chemical Property:

Melting Point:>97°C (dec.)
Storage Temp.:Refrigerator, Under Inert Atmosphere
Solubility.:Chloroform, Methanol

Purity/Quality:

95% ^*data from raw suppliers

2-(Acetylamino)-2-deoxy-β-D-galactopyranosylamine3,4,6-Triacetate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses 2-(Acetylamino)-2-deoxy-β-D-galactopyranosylamine 3,4,6-Triacetate is used in the synthesis of 1-N-(L-aspart-4-oyl)glycosylamines and their analogs.

Technology Process of 2-(AcetylaMino)-2-deoxy-β-D-galactopyranosylaMine 3,4,6-Triacetate

There total 8 articles about 2-(AcetylaMino)-2-deoxy-β-D-galactopyranosylaMine 3,4,6-Triacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 39541-20-3
1-azido 2-deoxy-2-acetamido 3,4,6-tri-O-acetyl-β-D-galactopyranoside

: 39541-22-5
(2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-aminotetrahydro-2H-pyran-3,4-diyl diacetate

Guidance literature:: With platinum(IV) oxide; hydrogen;

Reference yield:

: 3006-60-8
2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-galactopyranose

: 39541-22-5
(2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-aminotetrahydro-2H-pyran-3,4-diyl diacetate

Guidance literature:: Multi-step reaction with 3 steps

1: acetyl chloride

2: sodium azide; tetrabutylammonium hydrogen sulfate

3: hydrogen; platinum(IV) oxide

With platinum(IV) oxide; sodium azide; tetrabutylammonium hydrogen sulfate; hydrogen; acetyl chloride;

Reference yield:

: 39541-21-4
1-bromo-2-deoxy-2-acetamido-3,4,6-tri-O-acetyl-β-D-galactopyranoside

: 39541-22-5
(2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-aminotetrahydro-2H-pyran-3,4-diyl diacetate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium azide; tetra(n-butyl)ammonium hydrogensulfate / dichloromethane; water / 1 h

2: hydrogen; palladium on activated charcoal / ethyl acetate / 1 h / 20 °C

With sodium azide; palladium on activated charcoal; hydrogen; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; water; ethyl acetate;