(2R,3S,4R,5R)-2-(aminomethyl)oxane-2,3,4,5-tetrol

Base Information

Chemical Name:(2R,3S,4R,5R)-2-(aminomethyl)oxane-2,3,4,5-tetrol
CAS No.:4429-04-3
Molecular Formula:C6H13NO5
Molecular Weight:179.173
Hs Code.:
Nikkaji Number:J8.722J
ChEMBL ID:CHEMBL1742939
Mol file:4429-04-3.mol

Synonyms:Fructose,1-amino-1-deoxy-, D- (8CI);1-Amino-1-deoxy-D-fructose;D-Isoglucosamine;Fructosamine;

Suppliers and Price of (2R,3S,4R,5R)-2-(aminomethyl)oxane-2,3,4,5-tetrol

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 12 raw suppliers

Chemical Property of (2R,3S,4R,5R)-2-(aminomethyl)oxane-2,3,4,5-tetrol

Chemical Property:

Vapor Pressure:3.22E-07mmHg at 25°C
Refractive Index:1.64
Boiling Point:376.7 °C at 760 mmHg
Flash Point:181.6 °C
PSA：116.17000
Density:1.649 g/cm³
LogP:-2.55310
XLogP3:-3.5
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:179.07937252
Heavy Atom Count:12
Complexity:151

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(C(C(C(C(=O)CN)O)O)O)O
Isomeric SMILES:C([C@H]([C@H]([C@@H](C(=O)CN)O)O)O)O

Technology Process of (2R,3S,4R,5R)-2-(aminomethyl)oxane-2,3,4,5-tetrol

There total 12 articles about (2R,3S,4R,5R)-2-(aminomethyl)oxane-2,3,4,5-tetrol 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:

: 4429-04-3,27968-74-7,51296-39-0,93859-69-9,113532-32-4
inactive fructosamine

Guidance literature:: With acetic acid; zinc;

Reference yield:

: 23275-67-4
lyxo-[2]Hexosulose-bis-phenylhydrazon

: 64-19-7,77671-22-8
acetic acid

: 4429-04-3,27968-74-7,51296-39-0,93859-69-9,113532-32-4
inactive fructosamine

Guidance literature:: phenyl-α-acrosazone;

Reference yield:

: 82995-49-1
2-(D-arabino-tetraacetoxybutyl)-5-(3,4-diacetoxy-2-sulfobutyl)pyrazine

: 4429-04-3
1-amino-1-deoxy-D-fructose

Guidance literature:: Multi-step reaction with 2 steps

1: 4.1 g / HCl / ethanol

2: 7.5 mg / H₂, palladium oxide / aq. HCl / 16 h

With hydrogenchloride; palladium(II) oxide; hydrogen; In hydrogenchloride; ethanol;
DOI:10.1021/jo00145a034