alpha-L-sorbofuranose

Base Information

Chemical Name:alpha-L-sorbofuranose
CAS No.:36468-68-5
Molecular Formula:C6H12O6
Molecular Weight:180.158
Hs Code.:
UNII:VT8WK9DJ9Q
Metabolomics Workbench ID:57077
Nikkaji Number:J1.469.292D
Wikidata:Q27121302

Synonyms:alpha-L-sorbofuranose;VT8WK9DJ9Q;UNII-VT8WK9DJ9Q;36468-68-5;SCHEMBL4604138;.ALPHA.-L-SORBOFURANOSE;CHEBI:48647;Q27121302

Suppliers and Price of alpha-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
Packaging
price

Total 0 raw suppliers

Chemical Property of alpha-L-sorbofuranose

Chemical Property:

PSA：110.38000
LogP:-3.21980
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 alpha-L-sorbofuranose

There total 41 articles about alpha-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