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Lensiprazine

Base Information Edit
  • Chemical Name:Lensiprazine
  • CAS No.:327026-93-7
  • Molecular Formula:C24H27FN4O2
  • Molecular Weight:422.502
  • Hs Code.:
  • UNII:N47MW76OGX
  • DSSTox Substance ID:DTXSID60186379
  • Nikkaji Number:J2.489.039B
  • NCI Thesaurus Code:C83870
  • Pharos Ligand ID:2JPHYM24ZXZF
  • ChEMBL ID:CHEMBL196514
  • Mol file:327026-93-7.mol
Lensiprazine

Synonyms:8-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-4H-benzo(1,4)oxazin-2-methyl-3-one;SLV 314;SLV-314;SLV314

Suppliers and Price of Lensiprazine
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
  • LENSIPRAZINE 95.00%
  • 5G
  • $ 960.31
  • American Custom Chemicals Corporation
  • LENSIPRAZINE 95.00%
  • 2.5G
  • $ 824.49
  • American Custom Chemicals Corporation
  • LENSIPRAZINE 95.00%
  • 1G
  • $ 634.25
Total 21 raw suppliers
Chemical Property of Lensiprazine Edit
Chemical Property:
  • Boiling Point:668.468 °C at 760 mmHg 
  • PKA:12.51±0.40(Predicted) 
  • Flash Point:358.076 °C 
  • PSA:60.60000 
  • Density:1.263 g/cm3 
  • LogP:3.92210 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:5
  • Exact Mass:422.21180428
  • Heavy Atom Count:31
  • Complexity:629
Purity/Quality:

99% *data from raw suppliers

LENSIPRAZINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(=O)NC2=C(O1)C(=CC=C2)N3CCN(CC3)CCCC4=CNC5=C4C=C(C=C5)F
  • Isomeric SMILES:C[C@@H]1C(=O)NC2=C(O1)C(=CC=C2)N3CCN(CC3)CCCC4=CNC5=C4C=C(C=C5)F
Technology Process of Lensiprazine

There total 7 articles about Lensiprazine 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:

Reference yield: 58.0%

Guidance literature:
Guidance literature:
Multi-step reaction with 3 steps
1: H2 / Pd/C / ethanol; ethyl acetate / 24 h
2: chlorobenzene / 69 h / Heating
3: KI; DIPEA / acetonitrile / 18 h / Heating
With hydrogen; N-ethyl-N,N-diisopropylamine; potassium iodide; palladium on activated charcoal; In ethanol; ethyl acetate; chlorobenzene; acetonitrile;
DOI:10.1021/jm050148z
Guidance literature:
Multi-step reaction with 4 steps
1: 79 percent / Ph3P; DIAD / tetrahydrofuran / 96 h / 20 °C
2: H2 / Pd/C / ethanol; ethyl acetate / 24 h
3: chlorobenzene / 69 h / Heating
4: KI; DIPEA / acetonitrile / 18 h / Heating
With di-isopropyl azodicarboxylate; hydrogen; N-ethyl-N,N-diisopropylamine; triphenylphosphine; potassium iodide; palladium on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate; chlorobenzene; acetonitrile; 1: Mitsunobu reaction;
DOI:10.1021/jm050148z
Refernces Edit
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