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Parsalmide

Base Information Edit
  • Chemical Name:Parsalmide
  • CAS No.:30653-83-9
  • Molecular Formula:C14H18 N2 O2
  • Molecular Weight:246.309
  • Hs Code.:2924299090
  • European Community (EC) Number:250-274-2
  • UNII:YQH5093J7C
  • DSSTox Substance ID:DTXSID80865553
  • Nikkaji Number:J20.394G
  • Wikidata:Q27294664
  • NCI Thesaurus Code:C66326
  • ChEMBL ID:CHEMBL2107094
  • Mol file:30653-83-9.mol
Parsalmide

Synonyms:5-amino-N-butyl-2-(2-propynyloxy)benzamide;MY 41-6;MY-41-6;parsal;parsalmide

Suppliers and Price of Parsalmide
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
  • American Custom Chemicals Corporation
  • PARSALMIDE 95.00%
  • 5MG
  • $ 501.99
Total 2 raw suppliers
Chemical Property of Parsalmide Edit
Chemical Property:
  • Vapor Pressure:2.13E-07mmHg at 25°C 
  • Melting Point:83-85℃ 
  • Refractive Index:1.5500 (estimate) 
  • Boiling Point:424°Cat760mmHg 
  • PKA:pKa (aq soln, 20°) 4.6 ±0.03 
  • Flash Point:210.3°C 
  • PSA:64.35000 
  • Density:1.107g/cm3 
  • LogP:2.78280 
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:246.136827821
  • Heavy Atom Count:18
  • Complexity:308
Purity/Quality:

99% *data from raw suppliers

PARSALMIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCNC(=O)C1=C(C=CC(=C1)N)OCC#C
  • Therapeutic Function Muscle relaxant, Antiinflammatory, Analgesic
Technology Process of Parsalmide

There total 9 articles about Parsalmide 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 sulfuric acid; at 95 ℃; for 2h;
DOI:10.1016/S0223-5234(01)01251-X
Guidance literature:
With sodium tetrahydroborate; palladium 10% on activated carbon; In methanol; water; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.bmc.2012.06.026
Guidance literature:
Multi-step reaction with 4 steps
1.1: 79 percent / H2O / 0.25 h / 50 °C
2.1: 1-hydroxybenzotriazole; N,N'-dicyclohexylcarbodiimide / dimethylformamide / 0.5 h / 0 °C
2.2: 86 percent / dimethylformamide / 0 - 20 °C
3.1: 80 percent / NaOiPr / propan-2-ol / Heating
4.1: 90 percent / aq. H2SO4 / 2 h / 95 °C
With sulfuric acid; sodium isopropylate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In water; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/S0223-5234(01)01251-X
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