C₃₄H₂₆O₆

Base Information

Chemical Name:C₃₄H₂₆O₆
CAS No.:1286680-50-9
Molecular Formula:C₃₄H₂₆O₆
Molecular Weight:530.577
Hs Code.:

C<sub>34</sub>H<sub>26</sub>O<sub>6</sub>

Synonyms:

Suppliers and Price of C₃₄H₂₆O₆

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 C₃₄H₂₆O₆

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₄H₂₆O₆

There total 9 articles about C₃₄H₂₆O₆ 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:

: C₁₇H₁₄O₃

: 1286680-50-9
C₃₄H₂₆O₆

Guidance literature:: With copper(l) iodide; In N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.1002/ejoc.201001442

Reference yield:

: 916991-43-0
(2R,3S,4R)-3-(benzyloxy)-4-hydroxytetrahydrofuran-2-carbaldehyde

: 1286680-50-9
C₃₄H₂₆O₆

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / methanol / 20 °C

2: N-Bromosuccinimide; silver nitrate / acetone / 1.5 h / 20 °C

3: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; hydrogen; triethylamine / tetrahydrofuran / 2 h / 20 °C

4: N-Bromosuccinimide; silver fluoride / acetonitrile / 1.5 h / 20 °C

5: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; hydrogen; triethylamine / tetrahydrofuran / 2 h / 20 °C

6: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h / -78 °C

7: copper(l) iodide / N,N-dimethyl-formamide / 24 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; copper(l) iodide; tetrabutyl ammonium fluoride; hydrogen; silver fluoride; potassium carbonate; silver nitrate; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetone; acetonitrile; 3: Sonogashira coupling / 5: Sonogashira coupling;
DOI:10.1002/ejoc.201001442

Reference yield:

: 1286680-29-2
C₁₃H₁₄Br₂O₃

: 1286680-50-9
C₃₄H₂₆O₆

Guidance literature:: Multi-step reaction with 7 steps

1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -78 °C

2: N-Bromosuccinimide; silver nitrate / acetone / 1.5 h / 20 °C

3: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; hydrogen; triethylamine / tetrahydrofuran / 2 h / 20 °C

4: N-Bromosuccinimide; silver fluoride / acetonitrile / 1.5 h / 20 °C

5: copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; hydrogen; triethylamine / tetrahydrofuran / 2 h / 20 °C

6: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.08 h / -78 °C

7: copper(l) iodide / N,N-dimethyl-formamide / 24 h / 20 °C

With bis-triphenylphosphine-palladium(II) chloride; N-Bromosuccinimide; copper(l) iodide; tetrabutyl ammonium fluoride; hydrogen; silver fluoride; silver nitrate; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; N,N-dimethyl-formamide; acetone; acetonitrile; 3: Sonogashira coupling / 5: Sonogashira coupling;
DOI:10.1002/ejoc.201001442