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C43H59IN4O10

Base Information Edit
  • Chemical Name:C43H59IN4O10
  • CAS No.:382139-09-5
  • Molecular Formula:C43H59IN4O10
  • Molecular Weight:918.867
  • Hs Code.:
  • Mol file:382139-09-5.mol
C<sub>43</sub>H<sub>59</sub>IN<sub>4</sub>O<sub>10</sub>

Synonyms:C43H59IN4O10

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Chemical Property of C43H59IN4O10 Edit
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Technology Process of C43H59IN4O10

There total 23 articles about C43H59IN4O10 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:
Guidance literature:
With 4-pyrrolidin-1-ylpyridine; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/ja020091v
Guidance literature:
Multi-step reaction with 7 steps
1: 84 percent / triethylamine; DMAP / CH2Cl2 / 2.5 h
2: H2 / Pd/C / ethanol / 3 h / 2585.81 Torr
3: 385 mg / triethylamine; HBTU / acetonitrile / 1.5 h / 20 °C
4: H2 / Pd/C / ethanol / 4 h / 2585.81 Torr
5: 63 mg / triethylamine; HATU / acetonitrile / 3 h / 20 °C
6: lithium hydroxide monohydrate / tetrahydrofuran; H2O / 1 h / 0 °C
7: 4 mg / EDC; diisopropylethylamine; 4-pyrrolidinopyridine / CH2Cl2 / 0 - 20 °C
With dmap; lithium hydroxide; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; 4-pyrrolidin-1-ylpyridine; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1021/ja020091v
Guidance literature:
Multi-step reaction with 7 steps
1: 84 percent / triethylamine; DMAP / CH2Cl2 / 2.5 h
2: H2 / Pd/C / ethanol / 3 h / 2585.81 Torr
3: 385 mg / triethylamine; HBTU / acetonitrile / 1.5 h / 20 °C
4: H2 / Pd/C / ethanol / 4 h / 2585.81 Torr
5: 63 mg / triethylamine; HATU / acetonitrile / 3 h / 20 °C
6: lithium hydroxide monohydrate / tetrahydrofuran; H2O / 1 h / 0 °C
7: 4 mg / EDC; diisopropylethylamine; 4-pyrrolidinopyridine / CH2Cl2 / 0 - 20 °C
With dmap; lithium hydroxide; hydrogen; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; 4-pyrrolidin-1-ylpyridine; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; acetonitrile;
DOI:10.1021/ja020091v
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