D-Apio-alpha-L-furanose

Base Information

Chemical Name:D-Apio-alpha-L-furanose
CAS No.:41546-49-0
Molecular Formula:C5H10O5
Molecular Weight:150.131
Hs Code.:
UNII:3H2H67PLB1
Nikkaji Number:J35.079F
Mol file:41546-49-0.mol

Synonyms:D-Apio-alpha-L-furanose;3H2H67PLB1;UNII-3H2H67PLB1;41546-49-0;2,3,4-Furantriol, tetrahydro-4-(hydroxymethyl)-, (2R,3R,4S)-;D-APIO-.ALPHA.-L-FURANOSE

Suppliers and Price of D-Apio-alpha-L-furanose

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 D-Apio-alpha-L-furanose

Chemical Property:

XLogP3:-2.2
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:150.05282342
Heavy Atom Count:10
Complexity:127

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(C(C(O1)O)O)(CO)O
Isomeric SMILES:C1[C@]([C@H]([C@@H](O1)O)O)(CO)O

Technology Process of D-Apio-alpha-L-furanose

There total 128 articles about D-Apio-alpha-L-furanose 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:

: dihydrodehydrodiconiferyl alcohol 9-β-D-apiofuranosyl-(1→6)-β-D-glucopyranoside

: 492-61-5
β-D-glucose

: 20230-73-3,30738-01-3,30912-14-2,41546-43-4,41546-44-5,41546-45-6,41546-46-7,41546-47-8,41546-48-9,41546-49-0,41546-50-3,63865-04-3,36465-64-2
3-C-(hydroxymethyl)-β-D-erythrofuranose

Guidance literature:: With hydrogenchloride; In water; at 90 ℃; for 2h;
DOI:10.3390/molecules180910930

Reference yield:

: 3,4-dimethoxy-5-hydroxyphenyl β-D-apiofuranosyl(1→6)-β-D-glucopyranoside

: 492-61-5
β-D-glucose

: 20230-73-3,30738-01-3,30912-14-2,41546-43-4,41546-44-5,41546-45-6,41546-46-7,41546-47-8,41546-48-9,41546-49-0,41546-50-3,63865-04-3,36465-64-2
3-C-(hydroxymethyl)-β-D-erythrofuranose

Guidance literature:: With hydrogenchloride; In water; at 90 ℃; for 2h;
DOI:10.3390/molecules180910930

Reference yield:

: 6-hydroxymusizin 8-O-α-D-apiofuranosyl-(1→6)-β-D-glucopyranoside

: 6-methoxy-3-methyl-1,6,8-trihydroxy-2-naphthoic acid 8-O-β-D-glucopyranoside

: 492-62-6
alpha-D-glucopyranose

: 30738-01-3,30912-14-2,36465-64-2,41546-43-4,41546-44-5,41546-45-6,41546-46-7,41546-47-8,41546-48-9,41546-49-0,41546-50-3,63865-04-3,639-97-4,20230-73-3
D-apiose

Guidance literature:: 6-hydroxymusizin 8-O-α-D-apiofuranosyl-(1→6)-β-D-glucopyranoside; 6-methoxy-3-methyl-1,6,8-trihydroxy-2-naphthoic acid 8-O-β-D-glucopyranoside; With hydrogenchloride; In 1,4-dioxane; water; at 80 ℃; for 3h;

With pyridine; L-cysteine methyl ester hydrochloride; at 60 ℃; for 2h;

With 1-(Trimethylsilyl)imidazole; at 60 ℃; for 1.5h;
DOI:10.1155/2018/4851439