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Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate

Base Information
  • Chemical Name:Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate
  • CAS No.:140927-13-5
  • Molecular Formula:C14H15 N O3
  • Molecular Weight:245.278
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID10576625
  • Mol file:140927-13-5.mol
Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate

Synonyms:140927-13-5;benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate;benzyl 5-oxo-2aza-bicyclo[2.2.1]heptance-2-carboxylate;5-Oxo-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid benzyl ester;MFCD17976821;5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylic acid phenylmethyl ester;2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-oxo-, phenylmethyl ester;GKBNRJQNBQXKON-UHFFFAOYSA-N;SCHEMBL927563;(1R,4R)-Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate;Benzyl5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate;DTXSID10576625;1400808-09-4;AMY24851;AKOS015918136;SB33352;AS-31174;SY240539;2-Cbz-2-azabicyclo[2.2.1]heptan-5-one;A3043;CS-0060539;EN300-1660886

Suppliers and Price of Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate
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
  • Packaging
  • price
  • Usbiological
  • 5-Oxo-2-azabicyclo[2.2.1]heptane-2-carboxylic Acid Phenylmethyl Ester
  • 250mg
  • $ 460.00
  • TRC
  • 5-Oxo-2-azabicyclo[2.2.1]heptane-2-carboxylicAcidPhenylmethylEster
  • 2.5g
  • $ 1320.00
  • Medical Isotopes, Inc.
  • 5-Oxo-2-azabicyclo[2.2.1]heptane-2-carboxylicAcidPhenylmethylEster
  • 250 mg
  • $ 650.00
  • Matrix Scientific
  • Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate
  • 1g
  • $ 900.00
  • Matrix Scientific
  • Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate
  • 5g
  • $ 2250.00
  • J&W Pharmlab
  • 5-Oxo-2-aza-bicyclo[2.2.1]heptane-2-carboxylicacidbenzylester 96%
  • 25g
  • $ 2998.00
  • Crysdot
  • Benzyl5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate 95+%
  • 5g
  • $ 911.00
  • Chemenu
  • benzyl5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate 95%
  • 5g
  • $ 860.00
  • Chemenu
  • benzyl5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate 95%
  • 1g
  • $ 202.00
  • Biosynth Carbosynth
  • Benzyl5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate
  • 1 g
  • $ 450.00
Total 35 raw suppliers
Chemical Property of Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:402.515oC at 760 mmHg 
  • PKA:-1.07±0.20(Predicted) 
  • Flash Point:197.234oC 
  • PSA:46.61000 
  • Density:1.284g/cm3 
  • LogP:1.92440 
  • Storage Temp.:2-8°C 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:245.10519334
  • Heavy Atom Count:18
  • Complexity:349
Purity/Quality:

99% *data from raw suppliers

5-Oxo-2-azabicyclo[2.2.1]heptane-2-carboxylic Acid Phenylmethyl Ester *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C2CC(=O)C1CN2C(=O)OCC3=CC=CC=C3
  • Uses 5-Oxo-2-azabicyclo[2.2.1]heptane-2-carboxylic Acid Phenylmethyl Ester is an intermediate in the synthesis of potent agonists of nicotinic acetylcholine receptors.
Technology Process of Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate

There total 8 articles about Benzyl 5-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate 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 chromium(VI) oxide; sulfuric acid; In acetone; for 0.5h;
DOI:10.1039/b106212n
Guidance literature:
With jones reagent; In acetone; for 3h; Ambient temperature;
DOI:10.1021/jm00090a006
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