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propyl 1H-pyrrole-2-carboxylate

Base Information
  • Chemical Name:propyl 1H-pyrrole-2-carboxylate
  • CAS No.:173908-62-8
  • Molecular Formula:C8H11NO2
  • Molecular Weight:153.181
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20604544
  • Wikidata:Q82502532
  • Mol file:173908-62-8.mol
propyl 1H-pyrrole-2-carboxylate

Synonyms:propyl 1H-pyrrole-2-carboxylate;173908-62-8;Propyl1H-pyrrole-2-carboxylate;1H-Pyrrole-2-carboxylicacid,propylester(9CI);SCHEMBL9496881;Pyrrol-2-carbonsaure-propylester;DTXSID20604544;AKOS022060336;SB63127

Suppliers and Price of propyl 1H-pyrrole-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
  • Crysdot
  • Propyl1H-pyrrole-2-carboxylate 97%
  • 10g
  • $ 1687.00
  • Crysdot
  • Propyl1H-pyrrole-2-carboxylate 97%
  • 5g
  • $ 1240.00
  • Crysdot
  • Propyl1H-pyrrole-2-carboxylate 97%
  • 1g
  • $ 495.00
Total 1 raw suppliers
Chemical Property of propyl 1H-pyrrole-2-carboxylate
Chemical Property:
  • PSA:42.09000 
  • LogP:1.58150 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:153.078978594
  • Heavy Atom Count:11
  • Complexity:136
Purity/Quality:

Propyl1H-pyrrole-2-carboxylate 97% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCOC(=O)C1=CC=CN1
Technology Process of propyl 1H-pyrrole-2-carboxylate

There total 1 articles about propyl 1H-pyrrole-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 diethyl ether;
Guidance literature:
With potassium hydroxide;
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) t-BuOK, 18-crown-6 / 1.) THF, 15 min, 2.) THF, RT, 3.5 h
2: 90 percent / iron power, glacial acetic acid / 2 h / 60 °C
With 18-crown-6 ether; potassium tert-butylate; iron; acetic acid;
DOI:10.1021/jm950568w
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