C₆₀H₇₄N₄O₆Si

Base Information

Chemical Name:C₆₀H₇₄N₄O₆Si
CAS No.:1392212-62-2
Molecular Formula:C₆₀H₇₄N₄O₆Si
Molecular Weight:975.356
Hs Code.:

C<sub>60</sub>H<sub>74</sub>N<sub>4</sub>O<sub>6</sub>Si

Synonyms:

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Chemical Property of C₆₀H₇₄N₄O₆Si

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Technology Process of C₆₀H₇₄N₄O₆Si

There total 9 articles about C₆₀H₇₄N₄O₆Si 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: 91.0%

: 1374647-08-1
C₂₁H₃₁N₃O₂

: 1374647-12-7
C₃₉H₄₅NO₅Si

: 1392212-62-2
C₆₀H₇₄N₄O₆Si

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.02.027

Reference yield:

: 611-95-0
4-carboxybenzophenone

: 1392212-62-2
C₆₀H₇₄N₄O₆Si

Guidance literature:: Multi-step reaction with 4 steps

1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

2: water; lithium hydroxide / 1,2-dimethoxyethane

3: 1H-imidazole / N,N-dimethyl-formamide

4: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With 1H-imidazole; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In 1,2-dimethoxyethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.02.027

Reference yield:

: 98737-42-9
(4R,5R)-3-benzyl-5-{(1S)-1-[(tert-butoxycarbonyl)amino]-2-phenylethyl}dihydrofuran-2-(3H)-one

: 1392212-62-2
C₆₀H₇₄N₄O₆Si

Guidance literature:: Multi-step reaction with 5 steps

1: trifluoroacetic acid / dichloromethane / 20 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

3: water; lithium hydroxide / 1,2-dimethoxyethane

4: 1H-imidazole / N,N-dimethyl-formamide

5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide

With 1H-imidazole; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hydroxide; In 1,2-dimethoxyethane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.02.027