2-O-Methyl-beta-D-xylopyranose

Base Information

Chemical Name:2-O-Methyl-beta-D-xylopyranose
CAS No.:18652-95-4
Molecular Formula:C₆H₁₂O₅
Molecular Weight:164.158
Hs Code.:
UNII:L4X4SWZ5CU
Nikkaji Number:J1.849.197D

Synonyms:2-O-Methyl-beta-D-xylopyranose;L4X4SWZ5CU;UNII-L4X4SWZ5CU;beta-D-Xylopyranose, 2-O-methyl-;18652-95-4;SCHEMBL1547313;2-O-METHYL-.BETA.-D-XYLOPYRANOSE;.BETA.-D-XYLOPYRANOSE, 2-O-METHYL-

Suppliers and Price of 2-O-Methyl-beta-D-xylopyranose

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 2-O-Methyl-beta-D-xylopyranose

Chemical Property:

XLogP3:-2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:164.06847348
Heavy Atom Count:11
Complexity:128

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1C(C(COC1O)O)O
Isomeric SMILES:CO[C@@H]1[C@H]([C@@H](CO[C@H]1O)O)O

Technology Process of 2-O-Methyl-beta-D-xylopyranose

There total 6 articles about 2-O-Methyl-beta-D-xylopyranose 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: 66.7%

: 79936-18-8
benzyl 2-O-methyl-β-L-arabinopyranoside

: 18652-95-4,26685-78-9,27963-88-8,29198-39-8,32087-38-0,80299-47-4,86117-07-9,86117-08-0
2-O-methyl-L-arabinose

Guidance literature:: With hydrogen; dipyridinium dichromate; In ethanol; for 5h; Ambient temperature;

Reference yield:

: 79936-12-2
benzyl endo-3,4-O-benzylidene-β-L-arabinopyranoside

: 18652-95-4,26685-78-9,27963-88-8,29198-39-8,32087-38-0,80299-47-4,86117-07-9,86117-08-0
2-O-methyl-L-arabinose

Guidance literature:: Multi-step reaction with 3 steps

1: 93.9 percent / silver oxide / dimethylformamide / 10 h / Ambient temperature

2: 63.4 percent / 0.1 N sulfuric acid / ethanol / 4 h / Heating

3: 66.7 percent / H₂ / 10 percent PdC / ethanol / 5 h / Ambient temperature

With sulfuric acid; hydrogen; silver(l) oxide; dipyridinium dichromate; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 79936-14-4
benzyl endo-3,4-O-benzylidene-2-O-methyl-β-L-arabinopyranoside

: 18652-95-4,26685-78-9,27963-88-8,29198-39-8,32087-38-0,80299-47-4,86117-07-9,86117-08-0
2-O-methyl-L-arabinose

Guidance literature:: Multi-step reaction with 2 steps

1: 63.4 percent / 0.1 N sulfuric acid / ethanol / 4 h / Heating

2: 66.7 percent / H₂ / 10 percent PdC / ethanol / 5 h / Ambient temperature

With sulfuric acid; hydrogen; dipyridinium dichromate; In ethanol;