C₅₂H₄₈N₈O₁₂

Base Information

Chemical Name:C₅₂H₄₈N₈O₁₂
CAS No.:1355992-84-5
Molecular Formula:C₅₂H₄₈N₈O₁₂
Molecular Weight:977
Hs Code.:

C<sub>52</sub>H<sub>48</sub>N<sub>8</sub>O<sub>12</sub>

Synonyms:

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Chemical Property of C₅₂H₄₈N₈O₁₂

Chemical Property:

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Technology Process of C₅₂H₄₈N₈O₁₂

There total 12 articles about C₅₂H₄₈N₈O₁₂ 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:

: C₅₂H₅₀N₈O₁₃*(x)ClH

: 1355992-85-6
C₅₂H₄₈N₈O₁₂

: 1355992-84-5
C₅₂H₄₈N₈O₁₂

Guidance literature:: With dmap; diphenyl phosphoryl azide; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 8h;

Reference yield:

: 1095973-66-2
2-[(1S)-1-[[(1,1-dimethylethoxy)carbonyl]amino]-2-(phenylmethoxy)ethyl]-2-(4S)-oxazoline methyl ester

: 1355992-84-5
C₅₂H₄₈N₈O₁₂

Guidance literature:: Multi-step reaction with 8 steps

1: Bromotrichloromethane; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 4 h / 0 - 20 °C

2: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

3: N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate / dichloromethane / 3.5 h / 0 - 20 °C

4: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

5: N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate / dichloromethane / 3.5 h / 0 - 20 °C

6: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 10 h / 0 - 20 °C

7: hydrogenchloride / ethyl acetate / 6 h / 0 °C

8: dmap; diphenyl phosphoryl azide; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / dichloromethane / 8 h / 20 °C

With hydrogenchloride; dmap; lithium hydroxide monohydrate; Bromotrichloromethane; diphenyl phosphoryl azide; water; benzotriazol-1-ol; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;

Reference yield:

: 956111-99-2
2-((S)-2-benzyloxy-1-tert-butoxycarbonylaminoethyl)oxazole-4-carboxylic acid methyl ester

: 1355992-84-5
C₅₂H₄₈N₈O₁₂

Guidance literature:: Multi-step reaction with 7 steps

1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate / dichloromethane / 3.5 h / 0 - 20 °C

3: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 8 h / 0 - 20 °C

4: N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate / dichloromethane / 3.5 h / 0 - 20 °C

5: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 10 h / 0 - 20 °C

6: hydrogenchloride / ethyl acetate / 6 h / 0 °C

7: dmap; diphenyl phosphoryl azide; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / dichloromethane / 8 h / 20 °C

With hydrogenchloride; dmap; lithium hydroxide monohydrate; diphenyl phosphoryl azide; water; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;