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Levotofisopam

Base Information
  • Chemical Name:Levotofisopam
  • CAS No.:82059-51-6
  • Deprecated CAS:1232900-89-8
  • Molecular Formula:C22H26N2O4
  • Molecular Weight:382.459
  • Hs Code.:
  • UNII:11ZYL7QK34
  • Nikkaji Number:J2.362.969K
  • Wikidata:Q27251353
  • NCI Thesaurus Code:C76535
  • ChEMBL ID:CHEMBL2107351
  • Mol file:82059-51-6.mol
Levotofisopam

Synonyms:1-(3,4-dimethoxyphenyl)-5-ethyl-7,8-dimethoxy-4-methyl-5H-2,3-benzodiazepine;dextofisopam;EGYT-341;Grandaxin;levotofisopam;tofisopam;tofizopam

Suppliers and Price of Levotofisopam
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
Total 4 raw suppliers
Chemical Property of Levotofisopam
Chemical Property:
  • PSA:61.64000 
  • LogP:3.31270 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:6
  • Exact Mass:382.18925731
  • Heavy Atom Count:28
  • Complexity:579
Purity/Quality:

≥98% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1C(=NN=C(C2=CC(=C(C=C12)OC)OC)C3=CC(=C(C=C3)OC)OC)C
  • Isomeric SMILES:CC[C@@H]1C(=NN=C(C2=CC(=C(C=C12)OC)OC)C3=CC(=C(C=C3)OC)OC)C
  • Recent ClinicalTrials:Study of Levotofisopam 50 mg Three Times a Day (TID) Administered for 7 Days on Hyperuricemia and Gout
  • Uses Anxiolytic, autonomic instability.
Technology Process of Levotofisopam

There total 3 articles about Levotofisopam 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:
In acetonitrile; at 22 ℃; for 0.025 - 0.1h; Purification / work up;
Guidance literature:
With tofisopam; In methanol; acetonitrile; at 25 ℃; Purification / work up;

Reference yield:

Guidance literature:
In acetonitrile; Purification / work up;
upstream raw materials:

tofisopam

Downstream raw materials:

C4H6O6*C22H26N2O4

C22H25(2)HN2O4

tofisopam

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