Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside

Base Information

Chemical Name:Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside
CAS No.:88510-11-6
Molecular Formula:C₁₈H₂₆O₁₀
Molecular Weight:402.398
Hs Code.:
DSSTox Substance ID:DTXSID701195518
Nikkaji Number:J488.500G
Wikidata:Q105288239

Synonyms:DTXSID701195518;88510-11-6;Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside

Suppliers and Price of Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside

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 1 raw suppliers

Chemical Property of Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside

Chemical Property:

XLogP3:-2.2
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:7
Exact Mass:402.15259702
Heavy Atom Count:28
Complexity:473

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2C(C(C(C(O2)COC3C(C(C(O3)CO)O)O)O)O)O
Isomeric SMILES:C1=CC=C(C=C1)CO[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO[C@H]3[C@@H]([C@H]([C@@H](O3)CO)O)O)O)O)O

Technology Process of Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside

There total 4 articles about Phenylmethyl 6-O-alpha-L-arabinofuranosyl-beta-D-glucopyranoside 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: 98.0%

: 88510-15-0
benzyl 2,3,4-tri-O-acetyl-6-O-(2,3,5-tri-O-acetyl-α-L-arabinofuranosyl)-β-D-glucopyranoside

: 88510-11-6
phenylmethyl 6-O-α-L-arabinofuranosyl-(1->6)-β-D-glucopyranoside

Guidance literature:: With sodium methylate; In methanol; Ambient temperature;
DOI:10.1016/0008-6215(90)80004-M

Reference yield:

: 127243-79-2,127243-80-5,137432-11-2
2,3,4-tri-O-acetyl-6-O-(2,3,5-tri-O-acetyl-α-L-arabinofuranosyl)-α-D-glucopyranosly trichloroacetimidate

: 88510-11-6
phenylmethyl 6-O-α-L-arabinofuranosyl-(1->6)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / boron trifluoride etherate / benzene; CH₂Cl₂ / 2 h / Ambient temperature

2: 98 percent / sodium methoxide / methanol / Ambient temperature

With sodium methylate; boron trifluoride diethyl etherate; In methanol; dichloromethane; benzene;
DOI:10.1016/0008-6215(90)80004-M

Reference yield:

: 127243-78-1
2,3,4-tri-O-acetyl-6-O-(2,3,5-tri-O-acetyl-α-L-arabinofuranosyl)-β-D-glucopyranose

: 88510-11-6
phenylmethyl 6-O-α-L-arabinofuranosyl-(1->6)-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / K₂CO₃ / CH₂Cl₂ / 48 h / Ambient temperature

2: 83 percent / boron trifluoride etherate / benzene; CH₂Cl₂ / 2 h / Ambient temperature

3: 98 percent / sodium methoxide / methanol / Ambient temperature

With sodium methylate; potassium carbonate; boron trifluoride diethyl etherate; In methanol; dichloromethane; benzene;
DOI:10.1016/0008-6215(90)80004-M