N-1-naphthyl-3-nitrobenzamide

Base Information

Chemical Name:N-1-naphthyl-3-nitrobenzamide
CAS No.:63295-50-1
Molecular Formula:C₁₇H₁₂N₂O₃
Molecular Weight:292.294
Hs Code.:
DSSTox Substance ID:DTXSID70354466
Nikkaji Number:J1.885.121K
Wikidata:Q82132633
ChEMBL ID:CHEMBL1513660

Synonyms:N-1-naphthyl-3-nitrobenzamide;63295-50-1;N-(naphthalen-1-yl)-3-nitrobenzamide;N-(1-Naphthyl)-3-nitrobenzamide;N-naphthalen-1-yl-3-nitrobenzamide;N1-naphthyl-3-nitrobenzamide;MLS001194679;CHEMBL1513660;DTXSID70354466;3-Nitro-N-(1-naphthyl)benzamide;HMS2879L18;MFCD00409004;STK248722;AKOS001318326;SMR000554927;EU-0003114;SR-01000414953;SR-01000414953-1;Z28155798

Suppliers and Price of N-1-naphthyl-3-nitrobenzamide

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

American Custom Chemicals Corporation
N-NAPHTHALEN-1-YL-3-NITRO-BENZAMIDE 95.00%
5MG
$ 500.21

Total 1 raw suppliers

Chemical Property of N-1-naphthyl-3-nitrobenzamide

Chemical Property:

PSA：78.41000
LogP:4.90750
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:292.08479225
Heavy Atom Count:22
Complexity:421

Purity/Quality:: N-NAPHTHALEN-1-YL-3-NITRO-BENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Technology Process of N-1-naphthyl-3-nitrobenzamide

There total 2 articles about N-1-naphthyl-3-nitrobenzamide 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:

: 134-32-7
1-amino-naphthalene

: 121-90-4
m-nitrobenzoic acid chloride

: 63295-50-1
3-nitro-benzoic acid-[1]naphthylamide

Guidance literature:: With diethyl ether;

Reference yield:

: 121-92-6
3-nitrobenzoic acid

: 63295-50-1
3-nitro-benzoic acid-[1]naphthylamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂

2: Na₂CO₃ / diethyl ether

With thionyl chloride; sodium carbonate; In diethyl ether;
DOI:10.1039/b210106h