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Tetrazepam

Base Information Edit
  • Chemical Name:Tetrazepam
  • CAS No.:10379-14-3
  • Molecular Formula:C16H17 Cl N2 O
  • Molecular Weight:288.777
  • Hs Code.:
  • European Community (EC) Number:233-837-7
  • UNII:FO92091VP8
  • DSSTox Substance ID:DTXSID00146058
  • Nikkaji Number:J10.468J
  • Wikipedia:Tetrazepam
  • Wikidata:Q421104
  • NCI Thesaurus Code:C74282
  • Metabolomics Workbench ID:49703
  • ChEMBL ID:CHEMBL2105527
  • Mol file:10379-14-3.mol
Tetrazepam

Synonyms:4621 CB;Mobiforton;MTW-Tetrazepam;Musapam;Musaril;Myolastan;Myospasmal;Panos;Rilex;Tethexal;Tetra-saar;Tetramdura;Tetrarelax;Tetrazep 1A Pharma;Tetrazep AbZ;tetrazep von ct;tetrazepam

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of Tetrazepam Edit
Chemical Property:
  • Vapor Pressure:3.28E-10mmHg at 25°C 
  • Melting Point:144° 
  • Refractive Index:1.5800 (estimate) 
  • Boiling Point:502.1°Cat760mmHg 
  • PKA:4.10±0.10(Predicted) 
  • Flash Point:257.5°C 
  • PSA:32.34000 
  • Density:1.27g/cm3 
  • LogP:3.84130 
  • Solubility.:Practically insoluble in water, freely soluble in methylene chloride, soluble in acetonitrile. 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:288.1029409
  • Heavy Atom Count:20
  • Complexity:457
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1C(=O)CN=C(C2=C1C=CC(=C2)Cl)C3=CCCCC3
  • Uses Tetrazepam is a muscle relaxant (skeletal). This is a controlled substance (depressant).
  • Therapeutic Function Muscle relaxant
Technology Process of Tetrazepam

There total 1 articles about Tetrazepam 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:

Guidance literature:
Guidance literature:
With iron(II) sulfate; In acetonitrile; at 30 ℃; for 48h;
DOI:10.1002/jps.2600810216
Guidance literature:
With trifluoroacetic acid-d1; water-d2; In dimethylsulfoxide-d6; for 8h;
DOI:10.1002/jps.2600810216