C₅₆H₇₆O₁₇

Base Information

Chemical Name:C₅₆H₇₆O₁₇
CAS No.:163273-54-9
Molecular Formula:C₅₆H₇₆O₁₇
Molecular Weight:1021.21
Hs Code.:

C<sub>56</sub>H<sub>76</sub>O<sub>17</sub>

Synonyms:C₅₆H₇₆O₁₇

Suppliers and Price of C₅₆H₇₆O₁₇

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 C₅₆H₇₆O₁₇

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₆H₇₆O₁₇

There total 5 articles about C₅₆H₇₆O₁₇ 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: 72.0%

: 163125-40-4
(1'R,2'R)-Methyl 3,4-O-(1',2'-dimethoxycyclohexane-1',2'-diyl)-α-L-rhamnopyranoside

: 163273-53-8
(1S,3S,4R,4aR,8aR,9aS,10aR)-3-Ethylsulfanyl-8a,10a-dimethoxy-1-methyl-4-((2S,3R,4R,5S,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-decahydro-2,9,10-trioxa-anthracene

: 163273-54-9
C₅₆H₇₆O₁₇

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; 4 A molecular sieve; In diethyl ether; 1,2-dichloro-ethane; at 0 ℃;

Reference yield:

: 6014-42-2
L-rhamnose

: 163273-54-9
C₅₆H₇₆O₁₇

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) pyridine, 2.) BF₃*Et₂O

2: 94 percent / K₂CO₃ / methanol

3: 94 percent / NaH, TBAI / dimethylformamide

4: 59 percent / iodoniumdicollidine perchlorate, 4 Angstroem molecular sieves / 1,2-dichloro-ethane; diethyl ether / 0 deg C to r.t.

5: 72 percent / N-iodosuccinimide, CF₃SO₂OH, 4 Angstroem molecular sieves / 1,2-dichloro-ethane; diethyl ether / 0 °C

With pyridine; N-iodo-succinimide; trifluorormethanesulfonic acid; iodonium(di-γ-collidine) perchlorate; 4 A molecular sieve; boron trifluoride diethyl etherate; tetra-(n-butyl)ammonium iodide; sodium hydride; potassium carbonate; In methanol; diethyl ether; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 127753-94-0
ethyl 1-thio-α-L-rhamnopyranoside

: 163273-54-9
C₅₆H₇₆O₁₇

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / NaH, TBAI / dimethylformamide

2: 59 percent / iodoniumdicollidine perchlorate, 4 Angstroem molecular sieves / 1,2-dichloro-ethane; diethyl ether / 0 deg C to r.t.

3: 72 percent / N-iodosuccinimide, CF₃SO₂OH, 4 Angstroem molecular sieves / 1,2-dichloro-ethane; diethyl ether / 0 °C

With N-iodo-succinimide; trifluorormethanesulfonic acid; iodonium(di-γ-collidine) perchlorate; 4 A molecular sieve; tetra-(n-butyl)ammonium iodide; sodium hydride; In diethyl ether; 1,2-dichloro-ethane; N,N-dimethyl-formamide;