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1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester

Base Information Edit
  • Chemical Name:1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester
  • CAS No.:1270498-27-5
  • Molecular Formula:C14H20N2O2
  • Molecular Weight:248.325
  • Hs Code.:
  • Mol file:1270498-27-5.mol
1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester

Synonyms:benzyl 3-aminoazepane-1-carboxylate

Suppliers and Price of 1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Benzyl3-Aminoazepane-1-Carboxylate
  • 50mg
  • $ 220.00
  • Crysdot
  • Benzyl3-aminoazepane-1-carboxylate 95+%
  • 5g
  • $ 2456.00
  • Crysdot
  • Benzyl3-aminoazepane-1-carboxylate 95+%
  • 1g
  • $ 817.00
  • Chemenu
  • Benzyl3-aminoazepane-1-carboxylate 95%
  • 1g
  • $ 771.00
  • Alichem
  • Benzyl3-aminoazepane-1-carboxylate
  • 1g
  • $ 942.00
  • AK Scientific
  • benzyl3-aminoazepane-1-carboxylate
  • 100mg
  • $ 300.80
Total 3 raw suppliers
Chemical Property of 1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Benzyl3-Aminoazepane-1-Carboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester

There total 2 articles about 1H-Azepine-1-carboxylic acid, 3-aMinohexahydro-, phenylMethyl ester 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 [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; 2,4,6-Triisopropylthiophenol; ammonia; In methanol; toluene; at 20 ℃; for 16h; regioselective reaction; Inert atmosphere; Irradiation;
DOI:10.1002/chem.202003562
Guidance literature:
Multi-step reaction with 2 steps
1.1: lithium triethylborohydride / toluene; tetrahydrofuran / 0.75 h / -78 °C
1.2: 16 h / -78 - 20 °C
2.1: 2,4,6-Triisopropylthiophenol; [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; ammonia / toluene; methanol / 16 h / 20 °C / Inert atmosphere; Irradiation
With [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; 2,4,6-Triisopropylthiophenol; ammonia; lithium triethylborohydride; In tetrahydrofuran; methanol; toluene;
DOI:10.1002/chem.202003562
upstream raw materials:

N-(benzyloxycarbonyl)-2-oxo-azepane

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