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C35H38O6

Base Information Edit
C<sub>35</sub>H<sub>38</sub>O<sub>6</sub>

Synonyms:C35H38O6

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C35H38O6 Edit
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Technology Process of C35H38O6

There total 1 articles about C35H38O6 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:
Guidance literature:
C34H36O6; With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;
methyl iodide; In N,N-dimethyl-formamide; at 0 ℃; for 6h;
DOI:10.1039/c2cc17393j
Guidance literature:
With 20 % Pd(OH)2/C; hydrogen; acetic acid; In methanol; for 48h; under 60.006 Torr;
DOI:10.1039/c2cc17393j
Guidance literature:
Multi-step reaction with 2 steps
1: 20 % Pd(OH)2/C; hydrogen; acetic acid / methanol / 48 h / 60.01 Torr
2: Neisseria meningitidis CMP-sialic acid synthetase; cytidine 5′-triphosphate disodium salt; Pasteurella multocida sialic acid aldolase; Photobacterium damselae α2-6-sialyltransferase; magnesium chloride / pH 8.5 / aq. buffer; Enzymatic reaction
With Neisseria meningitidis CMP-sialic acid synthetase; cytidine 5′-triphosphate disodium salt; 20 % Pd(OH)2/C; Pasteurella multocida sialic acid aldolase; Photobacterium damselae α2-6-sialyltransferase; hydrogen; acetic acid; magnesium chloride; In methanol;
DOI:10.1039/c2cc17393j
upstream raw materials:

C34H36O6

methyl iodide

Downstream raw materials:

6-O-methyl-D-mannopyranose

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