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Benzetimide

Base Information
  • Chemical Name:Benzetimide
  • CAS No.:14051-33-3
  • Deprecated CAS:119391-55-8
  • Molecular Formula:C23H26 N2 O2
  • Molecular Weight:362.472
  • Hs Code.:2933399090
  • UNII:B987T0L5FX
  • DSSTox Substance ID:DTXSID2046173
  • Nikkaji Number:J8.476J
  • Wikidata:Q27274534
  • NCI Thesaurus Code:C73007
  • ChEMBL ID:CHEMBL10272
  • Mol file:14051-33-3.mol
Benzetimide

Synonyms:Benzetimide;Dexbenzetimid;Dexbenzetimide;Dexetimide;dextro Benzetimide;dextro-Benzetimide;R 16470;R-16470;R16470;Spasmentral;Tremblex

Suppliers and Price of Benzetimide
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
  • TRC
  • 1''-Benzyl-3-Phenyl-[3,4''-Bipiperidine]-2,6-Dione
  • 100mg
  • $ 310.00
  • TRC
  • 1''-Benzyl-3-Phenyl-[3,4''-Bipiperidine]-2,6-Dione
  • 50mg
  • $ 200.00
  • Matrix Scientific
  • 1'-Benzyl-3-phenyl-[3,4'-bipiperidine]-2,6-dione 98%
  • 5g
  • $ 1175.00
  • Matrix Scientific
  • 1'-Benzyl-3-phenyl-[3,4'-bipiperidine]-2,6-dione 98%
  • 1g
  • $ 595.00
  • Matrix Scientific
  • 1'-Benzyl-3-phenyl-[3,4'-bipiperidine]-2,6-dione 98%
  • 500mg
  • $ 387.00
Total 26 raw suppliers
Chemical Property of Benzetimide
Chemical Property:
  • Vapor Pressure:6.86E-12mmHg at 25°C 
  • Melting Point:156-159° 
  • Boiling Point:543.9°Cat760mmHg 
  • Flash Point:282.7°C 
  • PSA:49.41000 
  • Density:1.178g/cm3 
  • LogP:3.53990 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:362.199428076
  • Heavy Atom Count:27
  • Complexity:529
Purity/Quality:

99% *data from raw suppliers

1''-Benzyl-3-Phenyl-[3,4''-Bipiperidine]-2,6-Dione *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CN(CCC1C2(CCC(=O)NC2=O)C3=CC=CC=C3)CC4=CC=CC=C4
  • Use Description 3-(1-benzyl-4-piperidyl)-3-phenyl-piperidine-2,6-dione is a chemical compound with potential applications in various fields. In the field of pharmaceuticals and medicinal chemistry, it can serve as a key intermediate in the synthesis of organic molecules and pharmaceutical agents, potentially contributing to the development of new drugs targeting a range of medical conditions. Its role is pivotal in drug discovery and development, aiding in the creation of medications with specific therapeutic properties. Additionally, in the field of chemical research, 3-(1-benzyl-4-piperidyl)-3-phenyl-piperidine-2,6-dione can be employed as a reference compound for the study of piperidine derivatives and their reactivity, facilitating research in organic chemistry and chemical analysis. Furthermore, in the pharmaceutical industry, it may find applications as a chemical intermediate for the development of new drug compounds, potentially contributing to drug discovery and medicinal chemistry research. Its multifaceted utility underscores its significance in pharmaceuticals, chemical research, and scientific investigation, where it plays a crucial role in drug innovation, compound synthesis, and chemical analysis.
Technology Process of Benzetimide

There total 3 articles about Benzetimide 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 sodium hydrogencarbonate; In dichloromethane; water; at 20 ℃; for 18h;
Guidance literature:
With sulfuric acid; In acetic acid; at 165 ℃;
DOI:10.1016/j.bmcl.2008.07.115

Reference yield:

Guidance literature:
1-Benzyl-4-<α-cyan-α-(2-cyanethyl)-benzyl>-piperidin-hydrochlorid, konz. H2SO4;
DOI:10.1021/jm00310a607
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