4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl

Base Information

Chemical Name:4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl
CAS No.:346-99-6
Molecular Formula:C13H8F3NO2
Molecular Weight:267.207
Hs Code.:2904909090
DSSTox Substance ID:DTXSID10511672
Wikidata:Q82370578
Mol file:346-99-6.mol

Synonyms:346-99-6;4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl;1-(4-Nitrophenyl)-3-(trifluoromethyl)benzene;DTXSID10511672;GZNKLBNXFDXRRQ-UHFFFAOYSA-N;MFCD20529494;AKOS016001106;BS-28352;A874891

Suppliers and Price of 4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl

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

Crysdot
4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl 95+%
25g
$ 565.00

American Custom Chemicals Corporation
4'-NITRO-3-(TRIFLUOROMETHYL)-1,1'-BIPHENYL 95.00%
1G
$ 180.60

Alichem
4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl
25g
$ 605.26

AK Scientific
1-(4-Nitrophenyl)-3-(trifluoromethyl)benzene
1g
$ 131.00

Total 11 raw suppliers

Chemical Property of 4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:346.125oC at 760 mmHg
Flash Point:163.131oC
PSA：45.82000
Density:1.336g/cm3
LogP:4.80380
Storage Temp.:2-8°C
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:267.05071298
Heavy Atom Count:19
Complexity:319

Purity/Quality:

97% ^*data from raw suppliers

4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)C(F)(F)F)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of 4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl

There total 1 articles about 4'-Nitro-3-(trifluoromethyl)-1,1'-biphenyl 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: 63.0%

: 100-00-5
4-chlorobenzonitrile

: 1423-26-3
(meta-(trifluoromethyl)phenyl)boronic acid

: 346-99-6
4-nitro-3'-(trifluoromethyl)-1,1'-biphenyl

Guidance literature:: With tetrabutylammomium bromide; potassium carbonate; oxime-based palladacycle/polyvinylpyridine; In toluene; at 130 ℃; for 0.05h; microwave irradiation;
DOI:10.1055/s-2006-942370

Reference yield: 95.0%

: 346-99-6
4-nitro-3'-(trifluoromethyl)-1,1'-biphenyl

: 397-28-4
4-amino-3'-(trifluoromethyl)-1,1'-biphenyl

Guidance literature:: With tin(ll) chloride; In ethanol; ethyl acetate; Heating;
DOI:10.1016/S1383-5718(01)00345-X

Reference yield:

: 346-99-6
4-nitro-3'-(trifluoromethyl)-1,1'-biphenyl

: 454-92-2
3-(trifluoromethyl)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: tin; aq.-ethanolic HCl

2: KMnO₄; aqueous H₂SO₄ / 100 °C

With hydrogenchloride; tin; potassium permanganate; sulfuric acid;
DOI:10.1039/jr9510003459