Fadgg

Base Information

Chemical Name:Fadgg
CAS No.:124040-67-1
Molecular Formula:C₂₂H₃₈N₂O₁₅
Molecular Weight:570.548
Hs Code.:
DSSTox Substance ID:DTXSID40154197
Wikidata:Q83021348
Mol file:124040-67-1.mol

Synonyms:FADGG;O-fucopyranosyl-(1-3)-O-(2-acetamido-2-deoxyglucopyranosyl)-(1-6)-2-acetamido-2-deoxygalactopyranoside

Suppliers and Price of Fadgg

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 2 raw suppliers

Chemical Property of Fadgg

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:982.5°Cat760mmHg
Flash Point:548°C
PSA：273.17000
Density:1.58g/cm³
LogP:-4.57720
XLogP3:-5.3
Hydrogen Bond Donor Count:10
Hydrogen Bond Acceptor Count:15
Rotatable Bond Count:8
Exact Mass:570.22721851
Heavy Atom Count:39
Complexity:837

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C(C(C(C(O1)OC2C(C(OC(C2O)CO)OC3C(C(C(C(O3)CO)O)O)NC(=O)C)NC(=O)C)O)O)O
Isomeric SMILES:C[C@H]1[C@H]([C@H]([C@@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H](O[C@@H]([C@@H]2O)CO)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)NC(=O)C)NC(=O)C)O)O)O

Technology Process of Fadgg

There total 5 articles about Fadgg 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: 67.0%

: 124040-66-0
benzyl O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1->3)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

: 124040-67-1
O-α-L-fucopyranosyl-(1->3)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranose

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetic acid; for 48h; under 2587.7 Torr; Ambient temperature;
DOI:10.1016/0008-6215(89)84083-2

Reference yield:

: 33639-77-9
perbenzyl fucosyl bromide

: 124040-67-1
O-α-L-fucopyranosyl-(1->3)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranose

Guidance literature:: Multi-step reaction with 3 steps

1: 65 percent / ethyldiisopropylamine, molecular sieves / tetraethylammonium bromide / CH₂Cl₂ / 72 h / Ambient temperature

2: 82 percent / 60percent aq. AcOH / 0.25 h / 98 °C

3: 67 percent / H₂ / 10percent Pd/C / acetic acid / 48 h / 2587.7 Torr / Ambient temperature

With molecular sieve; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; tetraethylammonium bromide; In dichloromethane; acetic acid;
DOI:10.1016/0008-6215(89)84083-2

Reference yield:

: 85054-31-5
GlcNAc-β1,6-GalNAc-α1-OBn

: 124040-67-1
O-α-L-fucopyranosyl-(1->3)-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranose

Guidance literature:: Multi-step reaction with 4 steps

1: 68 percent / 4-toluenesulfonic acid monohydrate / dimethylformamide / 3 h / 70 °C

2: 65 percent / ethyldiisopropylamine, molecular sieves / tetraethylammonium bromide / CH₂Cl₂ / 72 h / Ambient temperature

3: 82 percent / 60percent aq. AcOH / 0.25 h / 98 °C

4: 67 percent / H₂ / 10percent Pd/C / acetic acid / 48 h / 2587.7 Torr / Ambient temperature

With molecular sieve; p-toluenesulfonic acid monohydrate; hydrogen; acetic acid; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; tetraethylammonium bromide; In dichloromethane; acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/0008-6215(89)84083-2