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1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI)

Base Information Edit
  • Chemical Name:1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI)
  • CAS No.:153602-58-5
  • Molecular Formula:C8H9NO3
  • Molecular Weight:167.164
  • Hs Code.:
  • Mol file:153602-58-5.mol
1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI)

Synonyms:1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI)

Suppliers and Price of 1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI)
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
  • AccelPharmtech
  • 3-acetyl-1H-Pyrrole-2-aceticacid 97.00%
  • 25G
  • $ 7320.00
  • AccelPharmtech
  • 3-acetyl-1H-Pyrrole-2-aceticacid 97.00%
  • 5G
  • $ 3900.00
  • AccelPharmtech
  • 3-acetyl-1H-Pyrrole-2-aceticacid 97.00%
  • 1G
  • $ 2280.00
Total 0 raw suppliers
Chemical Property of 1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI) Edit
Chemical Property:
  • PSA:70.16000 
  • LogP:0.84440 
Purity/Quality:

3-acetyl-1H-Pyrrole-2-aceticacid 97.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI)

There total 4 articles about 1H-Pyrrole-2-acetic acid, 3-acetyl- (9CI) 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 potassium hydroxide; In tetrahydrofuran; methanol; water; 1.) 0 deg C to r.t; 2.) 4 h, r.t.;
DOI:10.1016/S0040-4020(01)87212-4
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) oxalyl chloride / 1.) 1,2-dichloroethane, 15 min, r.t; 2.) 1,2-dichloroethane, 15 min, r.t.
2: 1.) aluminium chloride / 1.) 1,2-dichloroethane, 0 deg C to r.t, 10 min; 2.) 1,2-dichloroethane, nitromethane, 4 h, r.t; 0 deg C, 4 h
3: 96 percent / 5percent palladium on carbon / 1,3,5-trimethyl-benzene / 10 h / Heating
4: 88 percent / 2 M potassium hydroxide / tetrahydrofuran; methanol; H2O / 1.) 0 deg C to r.t; 2.) 4 h, r.t.
With potassium hydroxide; aluminium trichloride; oxalyl dichloride; palladium on activated charcoal; In tetrahydrofuran; methanol; water; 1,3,5-trimethyl-benzene;
DOI:10.1016/S0040-4020(01)87212-4
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / 5percent palladium on carbon / 1,3,5-trimethyl-benzene / 10 h / Heating
2: 88 percent / 2 M potassium hydroxide / tetrahydrofuran; methanol; H2O / 1.) 0 deg C to r.t; 2.) 4 h, r.t.
With potassium hydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; water; 1,3,5-trimethyl-benzene;
DOI:10.1016/S0040-4020(01)87212-4
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