C₄₈H₇₃N₅O₉

Base Information

Chemical Name:C₄₈H₇₃N₅O₉
CAS No.:1412893-38-9
Molecular Formula:C₄₈H₇₃N₅O₉
Molecular Weight:864.136
Hs Code.:

C<sub>48</sub>H<sub>73</sub>N<sub>5</sub>O<sub>9</sub>

Synonyms:

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Chemical Property of C₄₈H₇₃N₅O₉

Chemical Property:

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Technology Process of C₄₈H₇₃N₅O₉

There total 22 articles about C₄₈H₇₃N₅O₉ 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:

: 1412893-47-0
C₂₁H₃₈N₄O₇

: C₂₇H₃₇NO₃

: 1412893-38-9
C₄₈H₇₃N₅O₉

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.tetlet.2012.09.018

Reference yield:

: 19790-60-4
3-Benzyloxypropanal

: 1412893-38-9
C₄₈H₇₃N₅O₉

Guidance literature:: Multi-step reaction with 9 steps

1.1: titanium tetrachloride; (-)-sparteine / dichloromethane / 2 h / 0 °C

2.1: 2,6-dimethylpyridine / dichloromethane / 0.17 h / 0 °C

3.1: lithium borohydride / diethyl ether / 1 h / 0 °C

4.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C

4.2: -78 - 20 °C

5.1: n-butyllithium / tetrahydrofuran / -78 °C

6.1: methanol; camphor-10-sulfonic acid / dichloromethane

7.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 0 °C

8.1: trifluoroacetic acid / dichloromethane / 0 °C

9.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

With 2,6-dimethylpyridine; methanol; dmap; lithium borohydride; n-butyllithium; oxalyl dichloride; camphor-10-sulfonic acid; titanium tetrachloride; benzotriazol-1-ol; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; (-)-sparteine; In tetrahydrofuran; diethyl ether; dichloromethane; 5.1: |Wittig Olefination;
DOI:10.1016/j.tetlet.2012.09.018

Reference yield:

: C₁₈H₂₈O₂

: 1412893-38-9
C₄₈H₇₃N₅O₉

Guidance literature:: Multi-step reaction with 3 steps

1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 0 °C

2: trifluoroacetic acid / dichloromethane / 0 °C

3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 0 - 20 °C

With dmap; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/j.tetlet.2012.09.018