C₇₄H₁₂₂N₂O₁₀

Base Information

Chemical Name:C₇₄H₁₂₂N₂O₁₀
CAS No.:791805-44-2
Molecular Formula:C₇₄H₁₂₂N₂O₁₀
Molecular Weight:1199.79
Hs Code.:

C<sub>74</sub>H<sub>122</sub>N<sub>2</sub>O<sub>10</sub>

Synonyms:C₇₄H₁₂₂N₂O₁₀

Suppliers and Price of C₇₄H₁₂₂N₂O₁₀

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 C₇₄H₁₂₂N₂O₁₀

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₇₄H₁₂₂N₂O₁₀

There total 15 articles about C₇₄H₁₂₂N₂O₁₀ 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%

: 108-30-5
succinic acid anhydride

: C₇₀H₁₁₈N₂O₇

: 791805-44-2
C₇₄H₁₂₂N₂O₁₀

Guidance literature:: With pyridine; dmap; In dichloromethane; for 24h;
DOI:10.1021/jo0493020

Reference yield:

: 106-02-5,81031-90-5
pentadecanolide

: 791805-44-2
C₇₄H₁₂₂N₂O₁₀

Guidance literature:: Multi-step reaction with 10 steps

1.1: 87 percent / Amberlyst A-15 / 48 h / Heating

2.1: chlorotrimethylsilane / CH₂Cl₂ / 1.33 h / 20 °C

3.1: 82 percent / diisopropylethylamine; tetrabutylammonium iodide / tetrahydrofuran / 6 h / Heating

4.1: 91 percent / LiAlH₄ / tetrahydrofuran / Heating

5.1: NaH / tetrahydrofuran / 1 h / 0 °C

5.2: 90 percent / tetrabutylammonium iodide / tetrahydrofuran / 4 h / Heating

6.1: 100 percent / RuCl₂(=CHPh)(PCy₃)2 / CH₂Cl₂ / 48 h / Heating

7.1: BH₃*THF / tetrahydrofuran / 5 h / 0 - 20 °C

7.2: 70 percent / aq. NaOH; aq. H₂O₂ / tetrahydrofuran / 1 h / cooling

8.1: NaH / tetrahydrofuran / 2 h / Heating

8.2: 40 percent / tetrahydrofuran / Heating

9.1: triphenylphosphine grafted on polystyrene / tetrahydrofuran; H₂O / 20 - 25 °C

10.1: 72 percent / DMAP; pyridine / CH₂Cl₂ / 24 h

With pyridine; Grubbs catalyst first generation; dmap; lithium aluminium tetrahydride; chloro-trimethyl-silane; borane-THF; Amberlyst A-15; triphenylphosphine grafted on polystyrene; tetra-(n-butyl)ammonium iodide; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo0493020

Reference yield:

: 1611-56-9
1-Bromo-11-hydroxyundecane

: 791805-44-2
C₇₄H₁₂₂N₂O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaN₃

2.1: NaH / tetrahydrofuran / 2 h / Heating

2.2: 40 percent / tetrahydrofuran / Heating

3.1: triphenylphosphine grafted on polystyrene / tetrahydrofuran; H₂O / 20 - 25 °C

4.1: 72 percent / DMAP; pyridine / CH₂Cl₂ / 24 h

With pyridine; dmap; sodium azide; triphenylphosphine grafted on polystyrene; sodium hydride; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo0493020