alpha-L-fructofuranose

Base Information

Chemical Name:alpha-L-fructofuranose
CAS No.:41847-51-2
Molecular Formula:C₆H₁₂O₆
Molecular Weight:180.158
Hs Code.:
UNII:2K3JZZ40U4
Metabolomics Workbench ID:55675
Wikidata:Q27117242

Synonyms:alpha-L-fructofuranose;2K3JZZ40U4;UNII-2K3JZZ40U4;41847-51-2;alpha-l-fructose;.ALPHA.-L-FRUCTOFURANOSE;SCHEMBL15264856;CHEBI:37727;Q27117242

Suppliers and Price of alpha-L-fructofuranose

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
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price

Total 0 raw suppliers

Chemical Property of alpha-L-fructofuranose

Chemical Property:

XLogP3:-2.3
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:180.06338810
Heavy Atom Count:12
Complexity:162

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(C1C(C(C(O1)(CO)O)O)O)O
Isomeric SMILES:C([C@H]1[C@@H]([C@H]([C@](O1)(CO)O)O)O)O

Technology Process of alpha-L-fructofuranose

There total 40 articles about alpha-L-fructofuranose 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: 34.0%

: 2280-44-6
D-Glucose

: 67-47-0
5-hydroxymethyl-2-furfuraldehyde

: 470-23-5,470-24-6,10247-46-8,10489-79-9,35673-97-3,36441-90-4,36441-92-6,36468-68-5,37500-17-7,40461-86-7,40461-87-8,41579-20-8,41846-98-4,41846-99-5,41847-00-1,41847-01-2,41847-02-3,41847-03-4,41847-04-5,41847-05-6,41847-06-7,41847-51-2,41847-52-3,42744-42-3
D-fructose

Guidance literature:: With sodium chloride; In tetrahydrofuran; water; at 155 ℃; for 2h; Time; Temperature; chemoselective reaction; Inert atmosphere;
DOI:10.1039/c9nj01677e

Reference yield: 26.6%

: 492-62-6
alpha-D-glucopyranose

: 64-18-6
formic acid

: 3458-28-4
D-Mannose

: 470-23-5,470-24-6,10247-46-8,10489-79-9,35673-97-3,36441-90-4,36441-92-6,36468-68-5,37500-17-7,40461-86-7,40461-87-8,41579-20-8,41846-98-4,41846-99-5,41847-00-1,41847-01-2,41847-02-3,41847-03-4,41847-04-5,41847-05-6,41847-06-7,41847-51-2,41847-52-3,42744-42-3
D-fructose

Guidance literature:: With sodium aluminate; In N,N-dimethyl acetamide; water; at 60 ℃; for 0.75h; Autoclave;
DOI:10.1002/cctc.201501203

Reference yield: 5.0%

: 50-99-7
D-glucose

: 67-47-0
5-hydroxymethyl-2-furfuraldehyde

: 470-23-5,470-24-6,10247-46-8,10489-79-9,35673-97-3,36441-90-4,36441-92-6,36468-68-5,37500-17-7,40461-86-7,40461-87-8,41579-20-8,41846-98-4,41846-99-5,41847-00-1,41847-01-2,41847-02-3,41847-03-4,41847-04-5,41847-05-6,41847-06-7,41847-51-2,41847-52-3,42744-42-3
D-fructose

Guidance literature:: With chromium dichloride; [1,3-bis(2,4,6-trimethylphenyl)imidazol]-2-ylidene; In dimethyl sulfoxide; at 20 ℃; for 3h; Reagent/catalyst;
DOI:10.1021/cs500058p