benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Base Information

Chemical Name:benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside
CAS No.:95990-99-1
Molecular Formula:C₅₅H₈₃NO₉
Molecular Weight:902.265
Hs Code.:

Synonyms:benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Suppliers and Price of benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-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 0 raw suppliers

Chemical Property of benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

There total 7 articles about benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-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:

: 2862-10-4
benzyl-(2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside)

: 95990-99-1
benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / p-toluenesulfonic acid monohydrate / acetone / 4 h / Ambient temperature

2: 1.) palladium black, H₂, 2.) DMAP, DCC / 1.) MeOH, 6 h, atmospheric pressure, 2.) dichloromethane, 30 min, room temp.

3: 90percent acetic acid / 0.33 h / 90 °C

With dmap; hydrogen; toluene-4-sulfonic acid; palladium; acetic acid; dicyclohexyl-carbodiimide; In acetone;
DOI:10.1246/bcsj.60.2205

Reference yield:

: 3006-58-4,13030-01-8,42890-10-8,42973-23-9,77059-32-6,121785-09-9,7474-40-0
2-carbobenzyloxyamino-2-deoxy-D-glucopyranose

: 95990-99-1
benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 2.5percent dry HCl / 0.33 h / 100 °C

2: TsOH, CaSO₄ / acetone

3: hydrogen / Pd-black

4: DMAP, DCC / 0.5 h / Ambient temperature

5: 90percent AcOH / 0.17 h / 90 °C

With hydrogenchloride; dmap; calcium sulfate; hydrogen; toluene-4-sulfonic acid; acetic acid; dicyclohexyl-carbodiimide; palladium; In acetone;
DOI:10.1016/S0040-4039(00)61962-7

Reference yield:

: 100-51-6,185532-71-2
benzyl alcohol

: 95990-99-1
benzyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 2.5percent dry HCl / 0.33 h / 100 °C

2: TsOH, CaSO₄ / acetone

3: hydrogen / Pd-black

4: DMAP, DCC / 0.5 h / Ambient temperature

5: 90percent AcOH / 0.17 h / 90 °C

With hydrogenchloride; dmap; calcium sulfate; hydrogen; toluene-4-sulfonic acid; acetic acid; dicyclohexyl-carbodiimide; palladium; In acetone;
DOI:10.1016/S0040-4039(00)61962-7