beta-L-sorbofuranose

Base Information

Chemical Name:beta-L-sorbofuranose
CAS No.:41847-02-3
Molecular Formula:C₆H₁₂O₆
Molecular Weight:180.158
Hs Code.:
UNII:D58VFX69BN
Metabolomics Workbench ID:57078
Wikidata:Q27121303

Synonyms:beta-L-sorbofuranose;D58VFX69BN;UNII-D58VFX69BN;41847-02-3;.BETA.-L-SORBOFURANOSE;SCHEMBL15265620;CHEBI:48648;Q27121303

Suppliers and Price of beta-L-sorbofuranose

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 beta-L-sorbofuranose

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:: SDS file from LookChem

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 beta-L-sorbofuranose

There total 40 articles about beta-L-sorbofuranose 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