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Lerimazoline

Base Information Edit
  • Chemical Name:Lerimazoline
  • CAS No.:54765-26-3
  • Molecular Formula:C13H18N2
  • Molecular Weight:202.299
  • Hs Code.:
  • UNII:1YZY0ACA91
  • Nikkaji Number:J23.641A
  • Wikidata:Q27253243
  • NCI Thesaurus Code:C166525
  • Pharos Ligand ID:1DGQD312J2JT
  • ChEMBL ID:CHEMBL72178
  • Mol file:54765-26-3.mol
Lerimazoline

Synonyms:3-Pyridinecarboxamide, 2-chloro-N-(tetrahydro-2-oxo-3-thienyl)-;homocysteine-thiolactone-2-chloronicotinamide;ST 71;ST-71;ST71

Suppliers and Price of Lerimazoline
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
Total 1 raw suppliers
Chemical Property of Lerimazoline Edit
Chemical Property:
  • PSA:24.39000 
  • LogP:1.92040 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:202.146998583
  • Heavy Atom Count:15
  • Complexity:235
Purity/Quality:

98% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C(=C1)C)CC2=NCCN2)C
Technology Process of Lerimazoline

There total 3 articles about Lerimazoline 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 2 steps
1: HCl(gas) / diethyl ether / 0 - 20 °C
2: ethanol / 1.) 0 deg C, 1 h, 2.) reflux, 20 min
With hydrogenchloride; In diethyl ether; ethanol;
DOI:10.1021/jm970513p
Guidance literature:
Multi-step reaction with 3 steps
1: ethanol; H2O / 4 h / Heating
2: HCl(gas) / diethyl ether / 0 - 20 °C
3: ethanol / 1.) 0 deg C, 1 h, 2.) reflux, 20 min
With hydrogenchloride; In diethyl ether; ethanol; water;
DOI:10.1021/jm970513p

Reference yield:

Guidance literature:
DOI:10.1021/jm00235a020
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