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LP-261

Base Information
  • Chemical Name:LP-261
  • CAS No.:915412-67-8
  • Molecular Formula:C22H19N3O4S
  • Molecular Weight:421.477
  • Hs Code.:
  • UNII:O547O19Z01
  • Wikidata:Q27285346
  • Mol file:915412-67-8.mol
LP-261

Synonyms:LP 261;LP-261;LP261 cpd;N-(3-(1H-indol-4-yl)-5-(2-methoxyisonicotinoyl)phenyl)methanesulfonamide

Suppliers and Price of LP-261
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
  • American Custom Chemicals Corporation
  • LP-261 95.00%
  • 5MG
  • $ 495.77
Total 5 raw suppliers
Chemical Property of LP-261
Chemical Property:
  • PSA:109.53000 
  • LogP:4.99480 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:6
  • Exact Mass:421.10962727
  • Heavy Atom Count:30
  • Complexity:710
Purity/Quality:

97% *data from raw suppliers

LP-261 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=NC=CC(=C1)C(=O)C2=CC(=CC(=C2)C3=C4C=CNC4=CC=C3)NS(=O)(=O)C
Technology Process of LP-261

There total 7 articles about LP-261 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 5 steps
1.1: n-butyllithium / diethyl ether; hexane / -75 - -70 °C / Inert atmosphere
1.2: -75 - -71 °C / Inert atmosphere
1.3: -25 - 20 °C / Inert atmosphere
2.1: tetrakis(triphenylphosphine) palladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 18 h / 110 °C / Inert atmosphere
3.1: sodium / 18 h / 80 °C
4.1: potassium phosphate; 2’-(dimethylamino)-2-biphenylylpalladium(II) chloride dinorbornylphosphine complex / 1,4-dioxane; water / 100 °C / Inert atmosphere
5.1: tetrabutyl ammonium fluoride / tetrahydrofuran
With potassium phosphate; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; 2’-(dimethylamino)-2-biphenylylpalladium(II) chloride dinorbornylphosphine complex; tetrabutyl ammonium fluoride; sodium; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; diethyl ether; hexane; water; 4.1: Suzuki coupling;
DOI:10.1021/jm100659v
Guidance literature:
Multi-step reaction with 4 steps
1: tetrakis(triphenylphosphine) palladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene / 1,4-dioxane / 18 h / 110 °C / Inert atmosphere
2: sodium / 18 h / 80 °C
3: potassium phosphate; 2’-(dimethylamino)-2-biphenylylpalladium(II) chloride dinorbornylphosphine complex / 1,4-dioxane; water / 100 °C / Inert atmosphere
4: tetrabutyl ammonium fluoride / tetrahydrofuran
With potassium phosphate; tetrakis(triphenylphosphine) palladium(0); 2’-(dimethylamino)-2-biphenylylpalladium(II) chloride dinorbornylphosphine complex; tetrabutyl ammonium fluoride; sodium; caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; water; 3: Suzuki coupling;
DOI:10.1021/jm100659v
Guidance literature:
Multi-step reaction with 3 steps
1: sodium / 18 h / 80 °C
2: potassium phosphate; 2’-(dimethylamino)-2-biphenylylpalladium(II) chloride dinorbornylphosphine complex / 1,4-dioxane; water / 100 °C / Inert atmosphere
3: tetrabutyl ammonium fluoride / tetrahydrofuran
With potassium phosphate; 2’-(dimethylamino)-2-biphenylylpalladium(II) chloride dinorbornylphosphine complex; tetrabutyl ammonium fluoride; sodium; In tetrahydrofuran; 1,4-dioxane; water; 2: Suzuki coupling;
DOI:10.1021/jm100659v
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