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(3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth

Base Information
  • Chemical Name:(3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth
  • CAS No.:182561-27-9
  • Molecular Formula:C4H6O6*C16H22N2O3
  • Molecular Weight:440.45
  • Hs Code.:
  • Mol file:182561-27-9.mol
(3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth

Synonyms:(3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth;(3S)-3-Amino-2,3,4,5-Tetrahydro-2-Oxo-1h-1-Benzazepine-1-Acetatic Acid1,2-Dimethylethyl Ester, (2r,3r)-2,3-Dihydroxybutanedioate;(3S)-3-Amino-2,3,4,5-Tetrahydro-2-Oxo-1H-1-Benzazepine-1-AcetaticAcid1,2-DimethylethylEster,(2R,3R)-2,3-Dihydroxybutanedioate(1:1)

Suppliers and Price of (3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 18 raw suppliers
Chemical Property of (3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth
Chemical Property:
  • PSA:187.69000 
  • LogP:0.27750 
Purity/Quality:

98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of (3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth

There total 5 articles about (3S)-3-Amino-2,3,4,5-tetrahydro-2-oxo-1H-1-benzazepine-1-acetatic acid1,2-dimeth 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:
Multi-step reaction with 4 steps
1: 83 percent / dimethylformamide / 16 h / 60 °C
2: 93 percent / kalium-(tert-butylat) / dimethylformamide / 1 h / 0 - 5 °C
3: 85 percent / 2-aminoethanol / 0.08 h / 80 °C
4: 79 percent / C6H5CHO / ethanol / 14 h / Heating
With potassium tert-butylate; benzaldehyde; ethanolamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19880710205
Guidance literature:
Multi-step reaction with 3 steps
1: 93 percent / kalium-(tert-butylat) / dimethylformamide / 1 h / 0 - 5 °C
2: 85 percent / 2-aminoethanol / 0.08 h / 80 °C
3: 79 percent / C6H5CHO / ethanol / 14 h / Heating
With potassium tert-butylate; benzaldehyde; ethanolamine; In ethanol; N,N-dimethyl-formamide;
DOI:10.1002/hlca.19880710205
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