Mebenoside

Base Information

Chemical Name:Mebenoside
CAS No.:55902-93-7
Molecular Formula:C28H32 O6
Molecular Weight:464.558
Hs Code.:
UNII:3852AA20EI
Nikkaji Number:J34.153C
Wikidata:Q27256743
NCI Thesaurus Code:C83908
ChEMBL ID:CHEMBL3989484
Mol file:55902-93-7.mol

Synonyms:Mebenoside;Mebenosidum;55902-93-7;Mebenosido;Mebenoside [INN:DCF];Methyl 3,5,6-tri-O-benzyl-D-glucofuranoside;UNII-3852AA20EI;(3R,4R,5R)-5-[(1R)-1,2-bis(phenylmethoxy)ethyl]-2-methoxy-4-phenylmethoxyoxolan-3-ol;3852AA20EI;CB 28046;MEBENOSIDE [INN];SCHEMBL2733284;CHEMBL3989484;Q27256743;D-Glucofuranoside, methyl 3,5,6-tris-O-(phenylmethyl)-

Suppliers and Price of Mebenoside

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

American Custom Chemicals Corporation
MEBENOSIDE 95.00%
5MG
$ 505.34

Total 7 raw suppliers

Chemical Property of Mebenoside

Chemical Property:

Vapor Pressure:1.03E-15mmHg at 25°C
Boiling Point:609.6°Cat760mmHg
Flash Point:322.5°C
PSA：66.38000
Density:1.2g/cm³
LogP:4.10620
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:12
Exact Mass:464.21988874
Heavy Atom Count:34
Complexity:541

Purity/Quality:

99% ^*data from raw suppliers

MEBENOSIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1C(C(C(O1)C(COCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4)O
Isomeric SMILES:COC1[C@@H]([C@H]([C@H](O1)[C@@H](COCC2=CC=CC=C2)OCC3=CC=CC=C3)OCC4=CC=CC=C4)O

Technology Process of Mebenoside

There total 1 articles about Mebenoside 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:

: 67-56-1
methanol

: 35958-64-6
3,5,6-Tri-O-benzyl-D-glucofuranose

: 55902-93-7
methyl 3,5,6-tri-O-benzyl-α,β-D-glucofuranoside

Guidance literature:: With sulfuric acid; at 50 - 55 ℃; for 2h;

Reference yield: 99.0%

: 100-39-0
benzyl bromide

: 55902-93-7
methyl 3,5,6-tri-O-benzyl-α,β-D-glucofuranoside

: 201603-51-2
methyl 2,3,5,6-tetra-O-benzylglucofuranoside

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; for 5h; Ambient temperature;
DOI:10.1016/S0040-4039(97)10407-5

Reference yield: 93.7%

: 54533-84-5
2-(2-(2-chloroethoxy)ethoxy)tetrahydro-2H-pyran

: 20822-88-2,20822-89-3,55902-93-7
methyl 3,5,6-tri-O-benzyl-α-<*>-glucofuranoside

: 125365-35-7
Methyl 3,5,6-tri-O-benzyl-2-O-(2-tetrahydropyranyloxyethoxy)ethyl-β-<*>-glucofuranose

Guidance literature:: With 1H-imidazole; sodium hydride; tetra-(n-butyl)ammonium iodide; In N,N-dimethyl-formamide; 1.) NaH, Bu₄NI, imidazol, 2h, room temperatures, 2.) 2-chloroethoxyethyl tetrahydropyranyl ether, 5 days, room temperatures;
DOI:10.1016/0008-6215(89)84123-0