C₅₆H₈₀N₆O₁₀

Base Information

Chemical Name:C₅₆H₈₀N₆O₁₀
CAS No.:1399266-72-8
Molecular Formula:C₅₆H₈₀N₆O₁₀
Molecular Weight:997.285
Hs Code.:

C<sub>56</sub>H<sub>80</sub>N<sub>6</sub>O<sub>10</sub>

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₅₆H₈₀N₆O₁₀

Chemical Property:

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Technology Process of C₅₆H₈₀N₆O₁₀

There total 16 articles about C₅₆H₈₀N₆O₁₀ 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:

: 1399266-45-5
C₁₀H₁₀N₂O₄

: 1399266-69-3
C₄₆H₇₂N₄O₇*BrH

: 1399266-72-8
C₅₆H₈₀N₆O₁₀

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 22 ℃; for 18h; Inert atmosphere;
DOI:10.1039/c2ob26077h

Reference yield:

: 77629-24-4
benzyl cobactin T

: 1399266-72-8
C₅₆H₈₀N₆O₁₀

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 48 h / 22 °C / Inert atmosphere

2.1: dichloromethane / 0.25 h / 0 °C / Inert atmosphere

2.2: 1.75 h / 0 - 22 °C / Inert atmosphere

3.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 18 h / 22 °C / Inert atmosphere

With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1039/c2ob26077h

Reference yield:

: 1007123-22-9
(S)-1-(benzyloxy)-3-(benzyloxycarbonylamino)azepan-2-one

: 1399266-72-8
C₅₆H₈₀N₆O₁₀

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen bromide; acetic acid / dichloromethane

2.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / acetonitrile / 25 h / 22 °C / Inert atmosphere

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 48 h / 22 °C / Inert atmosphere

4.1: dichloromethane / 0.25 h / 0 °C / Inert atmosphere

4.2: 1.75 h / 0 - 22 °C / Inert atmosphere

5.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 18 h / 22 °C / Inert atmosphere

With dmap; hydrogen bromide; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; acetonitrile;
DOI:10.1039/c2ob26077h