N-[(E)-(3-nitrophenyl)methylideneamino]pyridine-4-carboxamide

Base Information

Chemical Name:N-[(E)-(3-nitrophenyl)methylideneamino]pyridine-4-carboxamide
CAS No.:16012-26-3
Molecular Formula:C₁₃H₁₀N₄O₃
Molecular Weight:270.247
Hs Code.:
European Community (EC) Number:659-473-2
DSSTox Substance ID:DTXSID601329344
ChEMBL ID:CHEMBL496758
Mol file:16012-26-3.mol

Synonyms:3-nitrobenzaldehyde isonicotinoylhydrazone

Suppliers and Price of N-[(E)-(3-nitrophenyl)methylideneamino]pyridine-4-carboxamide

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

Sigma-Aldrich
4-PYRIDINECARBOXYLIC (3-NITROBENZYLIDENE)HYDRAZIDE Aldrich
1ea
$ 57.00

Total 3 raw suppliers

Chemical Property of N-[(E)-(3-nitrophenyl)methylideneamino]pyridine-4-carboxamide

Chemical Property:

Melting Point:223-226 °C
PKA:10.57±0.46(Predicted)
Density:1.33±0.1 g/cm3(Predicted)
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:270.07529019
Heavy Atom Count:20
Complexity:374

Purity/Quality:

99% ^*data from raw suppliers

4-PYRIDINECARBOXYLIC (3-NITROBENZYLIDENE)HYDRAZIDE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC(=C1)[N+](=O)[O-])C=NNC(=O)C2=CC=NC=C2
Isomeric SMILES:C1=CC(=CC(=C1)[N+](=O)[O-])/C=N/NC(=O)C2=CC=NC=C2

Technology Process of N-[(E)-(3-nitrophenyl)methylideneamino]pyridine-4-carboxamide

There total 2 articles about N-[(E)-(3-nitrophenyl)methylideneamino]pyridine-4-carboxamide 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: 92.0%