(2S,3S,4R,5R)-5-amino-2,3,4,6-tetrahydroxyhexanoic acid

Base Information

Chemical Name:(2S,3S,4R,5R)-5-amino-2,3,4,6-tetrahydroxyhexanoic acid
CAS No.:62362-63-4
Molecular Formula:C6H13NO6
Molecular Weight:195.1705
Hs Code.:2933790090
DSSTox Substance ID:DTXSID50977910
Wikidata:Q82963222
Mol file:62362-63-4.mol

Synonyms:mannonic-delta-lactam

Suppliers and Price of (2S,3S,4R,5R)-5-amino-2,3,4,6-tetrahydroxyhexanoic acid

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
D-Manno-γ-lactam
5mg
$ 150.00

Medical Isotopes, Inc.
D-Manno-γ-lactam
5 mg
$ 390.00

Biosynth Carbosynth
D-Mannono-D-lactam
10 mg
$ 315.00

Biosynth Carbosynth
D-Mannono-D-lactam
5 mg
$ 168.00

Biosynth Carbosynth
D-Mannono-D-lactam
2 mg
$ 89.30

American Custom Chemicals Corporation
D-MANNONO-D-LACTAM 95.00%
50MG
$ 1593.90

American Custom Chemicals Corporation
D-MANNONO-D-LACTAM 95.00%
5MG
$ 738.10

Total 3 raw suppliers

Chemical Property of (2S,3S,4R,5R)-5-amino-2,3,4,6-tetrahydroxyhexanoic acid

Chemical Property:

Vapor Pressure:1.44E-18mmHg at 25°C
Melting Point:169-170oC
Boiling Point:630.9°Cat760mmHg
Flash Point:335.4°C
PSA：130.25000
Density:1.662g/cm³
LogP:-3.79140
Storage Temp.:-20°C Freezer
Solubility.:Water
XLogP3:-5.9
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:195.07428713
Heavy Atom Count:13
Complexity:175

Purity/Quality:

97% ^*data from raw suppliers

D-Manno-γ-lactam ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(C(C(C(C(C(=O)O)O)O)O)N)O
Isomeric SMILES:C([C@H]([C@H]([C@@H]([C@@H](C(=O)O)O)O)O)N)O
Uses A potent inhibitor of rat epididymal alpha-mannosidase and of apricot ?-glucosidase.

Technology Process of (2S,3S,4R,5R)-5-amino-2,3,4,6-tetrahydroxyhexanoic acid

There total 24 articles about (2S,3S,4R,5R)-5-amino-2,3,4,6-tetrahydroxyhexanoic acid 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: 89.0%

: 118464-50-9
6-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-D-mannono-δ-lactam

: 62362-63-4,156857-10-2
D-Mannonolactam

Guidance literature:: With trifluoroacetic acid; In water; for 1h;
DOI:10.1016/0040-4020(89)80059-6

Reference yield: 85.0%

: 120027-72-7
(3aS,6R,7R,7aS)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-7-hydroxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyridin-4-one

: 62362-63-4,156857-10-2
D-Mannonolactam

Guidance literature:: With trifluoroacetic acid; In water;
DOI:10.1039/c39880001221

Reference yield: 84.0%

: 158349-24-7
(3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-<(benzyloxy)methyl>piperidin-2-one

: 62362-63-4,156857-10-2
D-Mannonolactam

Guidance literature:: With hydrogenchloride; hydrogen; palladium dihydroxide; palladium on activated charcoal; In methanol; ethanol; for 48h;
DOI:10.1016/S0040-4020(01)86715-6