beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)-

Base Information

Chemical Name:beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)-
CAS No.:124378-00-3
Molecular Formula:C₈H₁₇NO₆
Molecular Weight:223.226
Hs Code.:
DSSTox Substance ID:DTXSID60154295
Nikkaji Number:J1.188.392C
Wikidata:Q76279578
Mol file:124378-00-3.mol

Synonyms:N-beta-D-Glucopyranosylhydroxyethylamine;beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)-;N-(2-Hydroxyethyl)beta-D-glucopyranosylamine;124378-00-3;SCHEMBL679050;DTXSID60154295;2-(beta-D-Glucopyranosylamino)ethanol;LS-71648

Suppliers and Price of beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)-

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 1 raw suppliers

Chemical Property of beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)-

Chemical Property:

Vapor Pressure:4.16E-13mmHg at 25°C
Boiling Point:522.6°Cat760mmHg
Flash Point:269.9°C
Density:1.51g/cm³
XLogP3:-3
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:223.10558726
Heavy Atom Count:15
Complexity:192

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CO)NC1C(C(C(C(O1)CO)O)O)O
Isomeric SMILES:C(CO)N[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O

Technology Process of beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)-

There total 5 articles about beta-D-Glucopyranosylamine, N-(2-hydroxyethyl)- 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: 91.3%

: 2280-44-6
D-Glucose

: 141-43-5
ethanolamine

: 124378-00-3
glucose β-hydroxyethylimine

Guidance literature:: In methanol; at 50 ℃; for 7h;
DOI:10.1016/j.carres.2008.07.005

Reference yield: 79.0%

: 50-99-7
D-glucose

: 141-43-5
ethanolamine

: 124378-00-3
glucose β-hydroxyethylimine

Guidance literature:: In ethanol; at 50 ℃; for 6h;
DOI:10.1007/BF02218768

Reference yield:

: 50-99-7
D-glucose

: 141-43-5
ethanolamine

: 124378-00-3
glucose β-hydroxyethylimine

: 124378-00-3
glucose β-hydroxyethylimine

Guidance literature:: In methanol; for 3h; Yield given; Yields of byproduct given. Title compound not separated from byproducts; Heating;
DOI:10.1007/BF02311327