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6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses

Base Information Edit
  • Chemical Name:6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses
  • CAS No.:1392816-07-7
  • Molecular Formula:C30H44N2O11
  • Molecular Weight:608.686
  • Hs Code.:
  • Mol file:1392816-07-7.mol
6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses

Synonyms:6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses

Suppliers and Price of 6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses Edit
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Technology Process of 6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses

There total 5 articles about 6,6'-di-O-(2-aminophenyl)-1',2,3,3',4,4'-hexa-O-methylsucroses 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 palladium 10% on activated carbon; hydrogen; In ethanol; ethyl acetate; at 20 ℃; for 12h;
DOI:10.1021/ol301993d
Guidance literature:
Multi-step reaction with 4 steps
1: ammonia; sodium / tetrahydrofuran / 2.33 h / -78 °C
2: triethylamine / dichloromethane / 1 h / 20 °C
3: potassium carbonate / N,N-dimethyl-formamide / 24 h / 100 °C
4: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 12 h / 20 °C
With palladium 10% on activated carbon; ammonia; hydrogen; sodium; potassium carbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ol301993d
Guidance literature:
Multi-step reaction with 4 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 12 h / 20 °C
2: triethylamine / dichloromethane / 1 h / 20 °C
3: potassium carbonate / N,N-dimethyl-formamide / 24 h / 100 °C
4: palladium 10% on activated carbon; hydrogen / ethanol; ethyl acetate / 12 h / 20 °C
With palladium 10% on activated carbon; tetrabutyl ammonium fluoride; hydrogen; potassium carbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ol301993d
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