Benzyl beta-l-arabinopyranoside

Base Information

• Chemical Name: Benzyl beta-l-arabinopyranoside
• CAS No.: 7473-38-3
• Molecular Formula: C12H16O5
• Molecular Weight: 240.256
• Hs Code.: 2932999099
• DSSTox Substance ID: DTXSID601296355
• Nikkaji Number: J81.404K
• Mol file: 7473-38-3.mol

Synonyms:Benzyl b-L-arabinopyranoside;7473-38-3;benzyl beta-l-arabinopyranoside;5329-50-0;BENZYL-BETA-L-ARABINOPYRANOSIDE;SCHEMBL7143032;CHEBI:188187;1-O-benzyl-beta-L-arabinopyranose;DTXSID601296355;BENZYLBETA-L-ARABINOPYRANOSIDE;Phenylmethyl beta-L-arabinopyranoside;(2S,3R,4S,5S)-2-phenylmethoxyoxane-3,4,5-triol;W-203010;(2S,3R,4S,5S)-2-(Benzyloxy)tetrahydro-2H-pyran-3,4,5-triol

Chemical Property of Benzyl beta-l-arabinopyranoside

Chemical Property:

• Boiling Point: 418.5°Cat760mmHg
• Flash Point: 206.9°C
• PSA: 79.15000
• Density: 1.35g/cm³
• LogP: -0.35780
• XLogP3: -0.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 240.09977361
• Heavy Atom Count: 17
• Complexity: 229

Purity/Quality:

99%, ^*data from raw suppliers

Benzylb-L-Arabinopyranoside ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(C(C(C(O1)OCC2=CC=CC=C2)O)O)O
• Isomeric SMILES: C1[C@@H]([C@@H]([C@H]([C@H](O1)OCC2=CC=CC=C2)O)O)O

Technology Process of Benzyl beta-l-arabinopyranoside

There total 9 articles about Benzyl beta-l-arabinopyranoside 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: 96.0%

L-arabinose (7296-55-1) + benzyl alcohol (100-51-6,185532-71-2) → benzyl β-L-arabinopyranoside (7473-38-3)

Guidance literature:

With hydrogenchloride; at 20 ℃; for 10h;

DOI:10.1016/j.bmc.2005.05.007

Reference yield: 91.0%

L-(+)-arabinose (87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2) + benzyl alcohol (100-51-6,185532-71-2) → benzyl β-L-arabinopyranoside (7473-38-3)

Guidance literature:

benzyl alcohol; With acetyl chloride; at 10 - 30 ℃; for 1.5h; Inert atmosphere;

L-(+)-arabinose; at 30 ℃; for 18h; Inert atmosphere;

Reference yield: 87.0%

L-arabinose (5328-37-0) + benzyl alcohol (100-51-6,185532-71-2) → benzyl β-L-arabinopyranoside (7473-38-3)

Guidance literature:

With acetyl chloride; at 20 ℃; for 120h;

DOI:10.1021/jo050928f

upstream raw materials:

L-(+)-arabinose

benzyl alcohol

L-arabinose

β-L-arabinopyranose

Downstream raw materials:

Benzyl-2,3,4-tri-O-acetyl-β-L-arabinopyranosid

(3aS,6S,7R,7aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-ol

benzyl 3,4-O-(S)-ethylidene-β-L-arabinopyranoside

benzyl 3,4-O-(S)-(1-phenylethylidene)-β-L-arabinopyranoside