6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

Base Information

Chemical Name:6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose
CAS No.:142037-63-6
Molecular Formula:C₁₇H₂₁NO₆S
Molecular Weight:367.423
Hs Code.:

Synonyms:6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

Suppliers and Price of 6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

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

Total 0 raw suppliers

Chemical Property of 6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

There total 1 articles about 6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose 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: 78.0%

: 141990-12-7
(1R,2R,3R)-N-benzenesulfonyl-N,O³-isopropylidene-1-(2-furyl)-2-aminobutane-1,3-diol

: 142037-63-6
6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

Guidance literature:: With sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;

Reference yield: 11.5%

: 142037-63-6
6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

: 74-88-4
methyl iodide

: 142037-59-0
methyl 6-(N-benzenesulfonylamino)-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-erythrooct-2-enopyranos-4-uloside

: methyl 6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-β-D-ribo-oct-2-enopyranosid-4-ulose

Guidance literature:: With silver(l) oxide; In diethyl ether; at 25 ℃; for 24h;

Reference yield:

: 142037-63-6
6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-oct-2-enopyranos-4-ulose

: methyl 6-amino-N-benzenesulfonyl-N,O-isopropylidene-2,3,6,8-tetradeoxy-α-D-ribo-octopyranosid-4-ulose

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / Ag₂O / diethyl ether / 24 h / 25 °C

2: 65 percent / 1.6 M diisobutylaluminum hydride / tetrahydrofuran / 0.5 h / -70 °C

With diisobutylaluminium hydride; silver(l) oxide; In tetrahydrofuran; diethyl ether;