5-(4-Nitrophenyl)isoxazole

Base Information

Chemical Name:5-(4-Nitrophenyl)isoxazole
CAS No.:3383-42-4
Molecular Formula:C9H6 N2 O3
Molecular Weight:190.158
Hs Code.:2934999090
DSSTox Substance ID:DTXSID00371808
Wikidata:Q82159262
Mol file:3383-42-4.mol

Synonyms:5-(4-Nitrophenyl)isoxazole;3383-42-4;5-(4-nitrophenyl)-1,2-oxazole;MFCD02183547;5-(p-nitro-phenyl)isoxazole;DTXSID00371808;AC5934;AKOS006229993;SY022833;CS-0308739;FT-0619670;EN300-129677;A875190;J-516272

Suppliers and Price of 5-(4-Nitrophenyl)isoxazole

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
5-(4-nitrophenyl)isoxazole
100mg
$ 65.00

Matrix Scientific
5-(4-Nitrophenyl)isoxazole
1g
$ 184.00

Crysdot
5-(4-Nitrophenyl)isoxazole 95+%
5g
$ 465.00

CHESS?
KG000109:5-(4-Nitro-phenyl)-isoxazole 95
5 g
$ 540.00

Chemenu
5-(4-Nitrophenyl)isoxazole 95%
5g
$ 439.00

American Custom Chemicals Corporation
5-(4-NITROPHENYL)ISOXAZOLE 95.00%
1G
$ 779.63

AK Scientific
5-(4-Nitrophenyl)isoxazole
5g
$ 1072.00

Total 8 raw suppliers

Chemical Property of 5-(4-Nitrophenyl)isoxazole

Chemical Property:

Vapor Pressure:2.24E-05mmHg at 25°C
Refractive Index:1.584
Boiling Point:371.2°Cat760mmHg
Flash Point:178.3°C
PSA：71.85000
Density:1.333g/cm³
LogP:2.77300
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:190.03784206
Heavy Atom Count:14
Complexity:209

Purity/Quality:

97% ^*data from raw suppliers

5-(4-nitrophenyl)isoxazole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 36/37/38
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=CC=NO2)[N+](=O)[O-]

Technology Process of 5-(4-Nitrophenyl)isoxazole

There total 9 articles about 5-(4-Nitrophenyl)isoxazole 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: 84.0%

: C₁₆H₁₄N₂O₂

: 3383-42-4
5-(4-nitrophenyl)isoxazole

Guidance literature:: With N-hydroxyphthalimide; [bis(acetoxy)iodo]benzene; In ethyl acetate; at 20 ℃; for 12h;
DOI:10.1016/j.tetlet.2018.04.062

Reference yield: 67.0%

: 78089-99-3
(E)-3-dimethylamino-1-(4-nitrophenyl)-2-propen-1-one

: 3383-42-4
5-(4-nitrophenyl)isoxazole

Guidance literature:: With hydroxylamine hydrochloride; In ethanol; at 78 ℃; for 16h;
DOI:10.1002/jhet.5570450337

Reference yield:

: 91869-61-3
1-[(E)-3-Dimethylamino-1-(4-nitro-phenyl)-prop-2-en-(E)-ylideneamino]-4,6-diphenyl-1H-pyridin-2-one

: 3383-42-4
5-(4-nitrophenyl)isoxazole

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / NH₂OH*HCl, CH₃ONa / methanol / 5 h / Heating

2: hydrochloric acid / methanol / 1 h / Heating

With hydrogenchloride; hydroxylamine hydrochloride; sodium methylate; In methanol;