1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3R,4R,5R,6S)-

Base Information

Chemical Name:1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3R,4R,5R,6S)-
CAS No.:130790-29-3
Molecular Formula:C6H13NO4
Molecular Weight:
Hs Code.:

Synonyms:

Suppliers and Price of 1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3R,4R,5R,6S)-

Supply Marketing:

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

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Chemical Property of 1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3R,4R,5R,6S)-

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3R,4R,5R,6S)-

There total 16 articles about 1H-Azepine-3,4,5,6-tetrol, hexahydro-, (3R,4R,5R,6S)- 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: 94.0%

: 20847-05-6,138332-00-0,138332-01-1
6-Azido-6-desoxy-D-glucopyranose

: 130790-29-3,280745-41-7
1,6-dideoxy-1,6-imino-(2S,3R,4R,5R)-D-glucitol

Guidance literature:: With hydrogen; palladium on activated charcoal; In water; for 48h; under 2585.7 Torr;
DOI:10.1021/ja960975c

Reference yield: 81.0%

: 551960-79-3
6-deoxy-6-N-benzyloxycarbonyl-1,2-O-isopropylidene-3-O-phenylmethyl-α-D-gluco-1,4-furanose

: 130790-29-3,280745-41-7
1,6-dideoxy-1,6-imino-(2S,3R,4R,5R)-D-glucitol

Guidance literature:: 6-deoxy-6-N-benzyloxycarbonyl-1,2-O-isopropylidene-3-O-phenylmethyl-α-D-gluco-1,4-furanose; With trifluoroacetic acid; In water; at 25 ℃; for 2.5h;

With hydrogen; palladium on activated charcoal; In hydrogenchloride; methanol; at 25 ℃; for 24h; under 4137.18 Torr;
DOI:10.1016/j.carres.2006.02.007