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4,4'-[(PhenylMethyl)iMino]bisbutanenitrile

Base Information Edit
  • Chemical Name:4,4'-[(PhenylMethyl)iMino]bisbutanenitrile
  • CAS No.:78217-67-1
  • Molecular Formula:C15H19N3
  • Molecular Weight:241.336
  • Hs Code.:
  • Mol file:78217-67-1.mol
4,4'-[(PhenylMethyl)iMino]bisbutanenitrile

Synonyms:N-benzyl-5-aza-nonanedinitrile;4,4'-[(Phenylmethyl)imino]bisbutanenitrile;1,7-dicyano-N-benzyl-4-azaheptane;5-benzyl-5-azanonanedinitrile;

Suppliers and Price of 4,4'-[(PhenylMethyl)iMino]bisbutanenitrile
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
  • TRC
  • 4,4''-[(Phenylmethyl)imino]bisbutanenitrile
  • 250mg
  • $ 275.00
  • Medical Isotopes, Inc.
  • 4,4??-[(Phenylmethyl)imino]bisbutanenitrile
  • 250 mg
  • $ 750.00
Total 3 raw suppliers
Chemical Property of 4,4'-[(PhenylMethyl)iMino]bisbutanenitrile Edit
Chemical Property:
  • PSA:50.82000 
  • LogP:3.09616 
  • Solubility.:DCM, Ethyl Acetate, Methanol 
Purity/Quality:

99% *data from raw suppliers

4,4''-[(Phenylmethyl)imino]bisbutanenitrile *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 4,4''-[(Phenylmethyl)imino]bisbutanenitrile is an intermediate in the synthesis of sym-Homospermidine (H625000), an analogue of Spermidine. sym-Homospermidine is used as an antineoplastic agent.
Technology Process of 4,4'-[(PhenylMethyl)iMino]bisbutanenitrile

There total 4 articles about 4,4'-[(PhenylMethyl)iMino]bisbutanenitrile 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 potassium carbonate; potassium iodide; In acetonitrile; for 16h; Reflux;
DOI:10.1074/jbc.M111.307835
Guidance literature:
With Ki; In diethyl ether; chloroform; toluene; butan-1-ol;
Guidance literature:
With potassium carbonate; In butan-1-ol; at 115 ℃;
DOI:10.1016/S0960-894X(03)00668-1
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