C₆₃H₇₀O₂₂

Base Information

Chemical Name:C₆₃H₇₀O₂₂
CAS No.:145835-83-2
Molecular Formula:C₆₃H₇₀O₂₂
Molecular Weight:1179.24
Hs Code.:

C<sub>63</sub>H<sub>70</sub>O<sub>22</sub>

Synonyms:

Suppliers and Price of C₆₃H₇₀O₂₂

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 C₆₃H₇₀O₂₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₆₃H₇₀O₂₂

There total 7 articles about C₆₃H₇₀O₂₂ 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:

: 98-88-4
benzoyl chloride

: 145835-83-2
C₆₃H₇₀O₂₂

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / 2 h / Ambient temperature

2: H₂ / 10percent Pd/C / acetic acid / 72 h / Ambient temperature

3: 1.) CCl₃CN, K₂CO₃ / 2.) TMSOTf / 1.) CH₂Cl₂, room temperature, 5 h, 2.) CH₂Cl₂, -20 deg C, 1 h

With pyridine; hydrogen; potassium carbonate; trichloroacetonitrile; palladium on activated charcoal; trimethylsilyl trifluoromethanesulfonate; In acetic acid;
DOI:10.1016/S0040-4039(00)60999-1

Reference yield:

: 138857-67-7
benzyl 2,3-di-O-benzoyl-4,6-O-<(S)-1-(methoxycarbonyl)ethylidene>-α-D-glucopyranoside

: 145835-83-2
C₆₃H₇₀O₂₂

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / MeOH / NaOMe / 24 h / Ambient temperature

2: 77 percent / imidazole / dimethylformamide / 1 h / Ambient temperature

4: pyridine / 2 h / Ambient temperature

5: H₂ / 10percent Pd/C / acetic acid / 72 h / Ambient temperature

6: 1.) CCl₃CN, K₂CO₃ / 2.) TMSOTf / 1.) CH₂Cl₂, room temperature, 5 h, 2.) CH₂Cl₂, -20 deg C, 1 h

With pyridine; 1H-imidazole; methanol; hydrogen; potassium carbonate; trichloroacetonitrile; palladium on activated charcoal; trimethylsilyl trifluoromethanesulfonate; sodium methylate; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)60999-1

Reference yield:

: 145835-75-2
benzyl 4,6-O-<(S)-1-(methoxycarbonyl)ethylidene>-α-D-glucopyranoside

: 145835-83-2
C₆₃H₇₀O₂₂

Guidance literature:: Multi-step reaction with 5 steps

1: 77 percent / imidazole / dimethylformamide / 1 h / Ambient temperature

3: pyridine / 2 h / Ambient temperature

4: H₂ / 10percent Pd/C / acetic acid / 72 h / Ambient temperature

5: 1.) CCl₃CN, K₂CO₃ / 2.) TMSOTf / 1.) CH₂Cl₂, room temperature, 5 h, 2.) CH₂Cl₂, -20 deg C, 1 h

With pyridine; 1H-imidazole; hydrogen; potassium carbonate; trichloroacetonitrile; palladium on activated charcoal; trimethylsilyl trifluoromethanesulfonate; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(00)60999-1