3-Nitro-9-fluorenone

Base Information

Chemical Name:3-Nitro-9-fluorenone
CAS No.:42135-22-8
Molecular Formula:C13H7NO3
Molecular Weight:225.203
Hs Code.:2914700090
European Community (EC) Number:255-675-6
NSC Number:90801
UNII:UCA2S9B5TS
DSSTox Substance ID:DTXSID9075325
Nikkaji Number:J1.049I
Wikidata:Q82003304
ChEMBL ID:CHEMBL354533
Mol file:42135-22-8.mol

Synonyms:3-nitro-9-fluorenone;3-nitrofluorenone

Suppliers and Price of 3-Nitro-9-fluorenone

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
3-Nitrofluorenone
250mg
$ 165.00

Medical Isotopes, Inc.
3-Nitrofluorenone
2.5 g
$ 2200.00

American Custom Chemicals Corporation
3-NITROFLUOREN-9-ONE 95.00%
100MG
$ 318.15

Total 7 raw suppliers

Chemical Property of 3-Nitro-9-fluorenone

Chemical Property:

Vapor Pressure:6.36E-08mmHg at 25°C
Melting Point:239.5°C
Refractive Index:1.4800 (estimate)
Boiling Point:439.5°Cat760mmHg
Flash Point:228.9°C
PSA：62.89000
Density:1.437g/cm³
LogP:3.32940
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:225.042593085
Heavy Atom Count:17
Complexity:349

Purity/Quality:

98%+ ^*data from raw suppliers

3-Nitrofluorenone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Other Classes -> Polycyclic Aromatic Hydrocarbons
Canonical SMILES:C1=CC=C2C(=C1)C3=C(C2=O)C=CC(=C3)[N+](=O)[O-]
Uses 3-Nitrofluorenone is a nitrated polycyclic aromatic hydrocarbon (PAH) with mutagenic activity.

Technology Process of 3-Nitro-9-fluorenone

There total 28 articles about 3-Nitro-9-fluorenone 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: 91.0%

: 124391-60-2
4-Nitro-2-phenylbenzoic acid

: 42135-22-8
3-nitro-9H-fluoren-9-one

Guidance literature:: With polyphosphoric acid; at 90 - 165 ℃; for 6h;
DOI:10.1016/j.bmcl.2018.03.081

Reference yield: 83.0%

: 486-25-9,952573-42-1
9-fluorenone

: 42135-22-8
3-nitro-9H-fluoren-9-one

Guidance literature:: With sulfuric acid; nitric acid; In water; at 80 - 90 ℃;

Reference yield: 65.0%

: 615-41-8
2-iodochlorobenzene

: 555-16-8
4-nitrobenzaldehdye

: 42135-22-8
3-nitro-9H-fluoren-9-one

Guidance literature:: With palladium diacetate; potassium hydrogencarbonate; DL-Pro-NHMe; In tert-Amyl alcohol; at 120 ℃; for 24h; Inert atmosphere;
DOI:10.1016/j.tet.2018.11.055