C₄₈H₅₀O₁₆

Base Information

Chemical Name:C₄₈H₅₀O₁₆
CAS No.:127588-75-4
Molecular Formula:C₄₈H₅₀O₁₆
Molecular Weight:882.915
Hs Code.:

C<sub>48</sub>H<sub>50</sub>O<sub>16</sub>

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₄₈H₅₀O₁₆

Chemical Property:

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Technology Process of C₄₈H₅₀O₁₆

There total 7 articles about C₄₈H₅₀O₁₆ 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: 51.0%

: 105376-04-3,138661-53-7,113214-71-4
ethyl 2,3,4,6-tetra-O-benzoyl-1-thio-β-D-glucopyranoside

: 122588-54-9
methyl 2,3:6,7-di-O-isopropylidene-L-glycero-α-D-manno-heptopyranoside

: 127588-75-4
C₄₈H₅₀O₁₆

Guidance literature:: With Phenylselenyl chloride; 4 A molecular sieve; silver trifluoromethanesulfonate; In 1,2-dichloro-ethane; for 0.0833333h;

Reference yield:

: 40653-15-4
methyl 2,3,4-tri-O-benzyl-α-D-manno-hexodialdo-1,5-pyranoside

: 127588-75-4
C₄₈H₅₀O₁₆

Guidance literature:: Multi-step reaction with 5 steps

1: tetrahydrofuran / 2 h / 0 °C

2: 1.) 20percent NH₄Cl; 2.) 30percent H₂O₂, NaHCO₃ / 1.) water, MeOH, THF, reflux, 15 h

3: 95 percent / H₂ / 10percent Pd/C / methanol

4: 85 percent / p-toluenesulphonic acid / acetone / 3 h / 20 °C

5: 51 percent / benzeneselenenyl chloride, 4 Angstroem molecular sieves, silver triflate / 1,2-dichloro-ethane / 0.08 h

With Phenylselenyl chloride; 4 A molecular sieve; hydrogen; dihydrogen peroxide; silver trifluoromethanesulfonate; sodium hydrogencarbonate; ammonium chloride; toluene-4-sulfonic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; 1,2-dichloro-ethane; acetone;

Reference yield:

: 122588-51-6
methyl-2,3,4-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside

: 127588-75-4
C₄₈H₅₀O₁₆

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / H₂ / 10percent Pd/C / methanol

2: 85 percent / p-toluenesulphonic acid / acetone / 3 h / 20 °C

3: 51 percent / benzeneselenenyl chloride, 4 Angstroem molecular sieves, silver triflate / 1,2-dichloro-ethane / 0.08 h

With Phenylselenyl chloride; 4 A molecular sieve; hydrogen; silver trifluoromethanesulfonate; toluene-4-sulfonic acid; palladium on activated charcoal; In methanol; 1,2-dichloro-ethane; acetone;