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[N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel

Base Information Edit
  • Chemical Name:[N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel
  • CAS No.:847654-17-5
  • Molecular Formula:C22H23 N3 Ni O3
  • Molecular Weight:436.133
  • Hs Code.:
  • European Community (EC) Number:678-458-1
  • Mol file:847654-17-5.mol
[N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel

Synonyms:847654-17-5;[N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel;N-[ALPHA-[2-(PIPERIDINOACETAMIDO)PHENYL]BENZYLIDENE]GLYCINATO]NICKEL;MFCD10566925;T72993;[N-[-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel

Suppliers and Price of [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel
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
  • TCI Chemical
  • [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel >93.0%(T)
  • 100mg
  • $ 40.00
  • TCI Chemical
  • [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel >93.0%(T)
  • 1g
  • $ 245.00
  • Chem-Impex
  • [N-[α-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel,≥93%(Assaybytitration) ≥93%(Assaybytitration)
  • 1G
  • $ 286.54
  • Chem-Impex
  • [N-[α-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel,93%(Assaybytitration) 93%(Assaybytitration)
  • 100MG
  • $ 47.04
  • Arctom
  • [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel 98%
  • 250mg
  • $ 76.00
  • Arctom
  • [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel 98%
  • 100mg
  • $ 32.00
  • Arctom
  • [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel 98%
  • 1g
  • $ 155.00
  • American Custom Chemicals Corporation
  • (N-(ALPHA-(2-(PIPERIDINOACETAMIDO)PHENYL)BENZYLIDENE)GLYCINATO)NICKEL 95.00%
  • 5MG
  • $ 502.04
  • AK Scientific
  • [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel
  • 100mg
  • $ 117.00
Total 7 raw suppliers
Chemical Property of [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel Edit
Chemical Property:
  • PSA:62.21000 
  • LogP:2.25320 
  • Solubility.:soluble in Chloroform 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:3
  • Exact Mass:436.117108
  • Heavy Atom Count:29
  • Complexity:558
Purity/Quality:

98% *data from raw suppliers

[N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel >93.0%(T) *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCN(CC1)CC(=O)[N-]C2=CC=CC=C2C(=NCC(=O)O)C3=CC=CC=C3.[Ni]
Technology Process of [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel

There total 3 articles about [N-[alpha-[2-(Piperidinoacetamido)phenyl]benzylidene]glycinato]nickel 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:
Multi-step reaction with 3 steps
1: potassium carbonate / acetonitrile / 1 h / 20 °C / Inert atmosphere
2: potassium carbonate / acetonitrile / 2 h / 60 °C / Inert atmosphere
3: potassium hydroxide / methanol / 60 - 70 °C
With potassium carbonate; potassium hydroxide; In methanol; acetonitrile;
DOI:10.1016/j.tet.2020.131741
Guidance literature:
Multi-step reaction with 2 steps
1: potassium carbonate / acetonitrile / 2 h / 60 °C / Inert atmosphere
2: potassium hydroxide / methanol / 60 - 70 °C
With potassium carbonate; potassium hydroxide; In methanol; acetonitrile;
DOI:10.1016/j.tet.2020.131741
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