alpha-L-arabinopyranose

Base Information

• Chemical Name: alpha-L-arabinopyranose
• CAS No.: 7296-55-1
• Molecular Formula: C5H10O5
• Molecular Weight: 150.131
• European Community (EC) Number: 201-767-6
• UNII: UO2PIV2K4C
• DSSTox Substance ID: DTXSID201315713
• Nikkaji Number: J82.114D
• Wikidata: Q27104583
• Metabolomics Workbench ID: 52453
• ChEMBL ID: CHEMBL505348
• Mol file: 7296-55-1.mol

Synonyms:alpha-L-arabinopyranose;7296-55-1;alpha-L-Arabinose;UO2PIV2K4C;(2R,3R,4S,5S)-oxane-2,3,4,5-tetrol;UNII-UO2PIV2K4C;Arabinopyranose, alpha-L-;CHEBI:46987;6abp;SCHEMBL112371;CHEMBL505348;.ALPHA.-L-ARABINOPYRANOSE;DTXSID201315713;87-72-9;ARABINOPYRANOSE, .ALPHA.-L-;C02604;Q27104583;(2R,3R,4S,5S)-Tetrahydro-2H-pyran-2,3,4,5-tetraol;WURCS=2.0/1,1,0/[a211h-1a_1-5]/1/

Chemical Property of alpha-L-arabinopyranose

Chemical Property:

• PSA: 90.15000
• LogP: -2.58230
• XLogP3: -2.5
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 150.05282342
• Heavy Atom Count: 10
• Complexity: 117

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Biological Agents -> Monosaccharides and Derivatives
• Canonical SMILES: C1C(C(C(C(O1)O)O)O)O
• Isomeric SMILES: C1[C@@H]([C@@H]([C@H]([C@@H](O1)O)O)O)O

Technology Process of alpha-L-arabinopyranose

There total 792 articles about alpha-L-arabinopyranose 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:

kaempferol 3-O-β-D-glucopyranosyl-(1'''→2'')-O-α-L-arabinopyranoside → β-D-glucose (492-61-5) + L-arabinose (7296-55-1)

Guidance literature:

With hydrogenchloride; In ethanol; at 80 ℃; for 2h;

DOI:10.3390/molecules19056727

Reference yield:

kaempferol 3-O-β-D-glucopyranosyl-(1'''→2'')-O-α-L-arabinopyranoside-7-O-β-D-glucopyranoside → β-D-glucose (492-61-5) + L-arabinose (7296-55-1)

Guidance literature:

With hydrogenchloride; In ethanol; at 80 ℃; for 2h;

DOI:10.3390/molecules19056727

Reference yield:

kaempferol 3-O-β-D-[6'''-O-(E-caffeoyl)]glucopyranosyl-(1'''→2'')-O-α-L-arabinopyranoside-7-O-β-D-glucopyranoside → β-D-glucose (492-61-5) + L-arabinose (7296-55-1)

Guidance literature:

With hydrogenchloride; In ethanol; at 80 ℃; for 2h;

DOI:10.3390/molecules19056727

upstream raw materials:

diazomethane

3-O-β-D-galactopyranosyl-(1->2)-<β-D-xylopyranosyl-(1->3)>-β-D-glucuronopyranosyl quillaic acid 28-O-β-D-apiofuranosyl-(1->3)-β-D-xylopyranosyl-(1->4)-<β-D-glucopyranosyl-(1->3)>-α-L-rhamnopyranosyl-(1->2)-β-D-fucopyranoside.

methanol

D-(+)-xylobiose

Downstream raw materials:

methyl xyloside

methyl-β-D-xylopyranoside

methyl-α-D-xylopyranoside

5-deoxy-1,2-O-isopropylidene-α-D-xylohexofuranose

Refernces

• 1、 Jiang, Pei-Jing,Lu, Mei-Jiao,Xi, Yi-Yuan,Chen, Jun,Zheng, Ju-Jia,Xu, Xiang-Wei. "New flavonoid glycosides from Xanthium strumarium with their protein tyrosine phosphatase 1B inhibitory activity". . p. 45 - 51. Retrieved 2021/01/25.
• 2、 Bier, Claus,Binder, Dennis,Bitzenhofer, Nora Lisa,Drepper, Thomas,Haase, Mona,Hilgers, Fabienne,Hogenkamp, Fabian,Jaeger, Karl-Erich,Ophoven, Vera,Pietruszka, J?rg. "Optochemical Control of Bacterial Gene Expression: Novel Photocaged Compounds for Different Promoter Systems". . . Retrieved 2021/12/06.