C₃₅H₄₁NO₁₀

Base Information

Chemical Name:C₃₅H₄₁NO₁₀
CAS No.:1415996-63-2
Molecular Formula:C₃₅H₄₁NO₁₀
Molecular Weight:635.711
Hs Code.:

C<sub>35</sub>H<sub>41</sub>NO<sub>10</sub>

Synonyms:C₃₅H₄₁NO₁₀

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Chemical Property of C₃₅H₄₁NO₁₀

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Technology Process of C₃₅H₄₁NO₁₀

There total 5 articles about C₃₅H₄₁NO₁₀ 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:

: C₃₄H₃₉NO₁₀

: 74-88-4
methyl iodide

: 1415996-63-2
C₃₅H₄₁NO₁₀

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1039/c2ob26928g

Reference yield:

: 460082-41-1
phenyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

: 1415996-63-2
C₃₅H₄₁NO₁₀

Guidance literature:: Multi-step reaction with 4 steps

1: N-iodo-succinimide; trifluorormethanesulfonic acid / dichloromethane / 5 h / -10 °C / Molecular sieve; Inert atmosphere

2: trifluoroacetic acid / dichloromethane; methanol / 0.5 h / 0 °C

3: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane; water / 6 h / 0 °C

4: potassium carbonate / N,N-dimethyl-formamide / 0 - 20 °C

With N-iodo-succinimide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; trifluorormethanesulfonic acid; [bis(acetoxy)iodo]benzene; potassium carbonate; trifluoroacetic acid; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1039/c2ob26928g

Reference yield:

: 1415996-61-0
N-benzyloxycarbonyl-6-aminohexyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside

: 1415996-63-2
C₃₅H₄₁NO₁₀

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / dichloromethane; methanol / 0.5 h / 0 °C

2: 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene / dichloromethane; water / 6 h / 0 °C

3: potassium carbonate / N,N-dimethyl-formamide / 0 - 20 °C

With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; [bis(acetoxy)iodo]benzene; potassium carbonate; trifluoroacetic acid; In methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1039/c2ob26928g