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N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide

Base Information Edit
  • Chemical Name:N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide
  • CAS No.:96426-93-6
  • Molecular Formula:C16H18BrN3O4S
  • Molecular Weight:428.307
  • Hs Code.:
  • Mol file:96426-93-6.mol
N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide

Synonyms:Eudistomine F;

Suppliers and Price of N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide
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Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:115.61000 
  • Density:1.74g/cm3 
  • LogP:3.03800 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide

There total 14 articles about N-[[(1S)-11-Bromo-1,2,7,8,13,13bβ-hexahydro-10-hydroxy[1,6,2]oxathiazepino[2',3':1,2]pyrido[3,4-b]indol]-1α-yl]-2-hydroxyacetamide 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 boron tribromide;
Guidance literature:
Multi-step reaction with 5 steps
1: CH2Cl2 / Ambient temperature
2: 96 percent / TFA / CH2Cl2 / 2 h / -78 °C
3: mCPBA
4: 22 percent / TsOH / CH2Cl2 / 2 h / Ambient temperature
5: 33 percent / BBr3
With boron tribromide; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In dichloromethane;
Guidance literature:
Multi-step reaction with 7 steps
1: iPr2NEt / CH2Cl2 / 1 h / Ambient temperature
2: DIBAL / toluene / 2 h / -78 °C
3: CH2Cl2 / Ambient temperature
4: 96 percent / TFA / CH2Cl2 / 2 h / -78 °C
5: mCPBA
6: 22 percent / TsOH / CH2Cl2 / 2 h / Ambient temperature
7: 33 percent / BBr3
With boron tribromide; diisobutylaluminium hydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In dichloromethane; toluene;
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