2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)-

Base Information

Chemical Name:2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)-
CAS No.:75745-64-1
Molecular Formula:C₁₁H₆N₂O₅S
Molecular Weight:278.245
Hs Code.:
DSSTox Substance ID:DTXSID60226628
Wikidata:Q83106104
Mol file:75745-64-1.mol

Synonyms:BRN 4514039;2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)-;75745-64-1;5-((4-Nitrophenyl)sulfonyl)-2-furancarbonitrile;C11H6N2O5S;DTXSID60226628;C11-H6-N2-O5-S;LS-70085

Suppliers and Price of 2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)-

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
5-((4-NITROPHENYL)SULFONYL)-2-FURANCARBONITRILE 95.00%
5MG
$ 498.45

Total 2 raw suppliers

Chemical Property of 2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)-

Chemical Property:

Vapor Pressure:1.41E-10mmHg at 25°C
Boiling Point:511.5°C at 760 mmHg
Flash Point:263.1°C
PSA：125.27000
Density:1.6g/cm³
LogP:3.49628
XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:277.99974247
Heavy Atom Count:19
Complexity:489

Purity/Quality:

98% ^*data from raw suppliers

5-((4-NITROPHENYL)SULFONYL)-2-FURANCARBONITRILE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1[N+](=O)[O-])S(=O)(=O)C2=CC=C(O2)C#N

Technology Process of 2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)-

There total 1 articles about 2-Furancarbonitrile, 5-((4-nitrophenyl)sulfonyl)- 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: 54.0%

: 75745-89-0
5-<(4-nitrophenyl)thio>-2-furancarbonitrile

: 75745-64-1
5-<(4-nitrophenyl)sulphonyl>-2-furancarbonitrile

Guidance literature:: With dihydrogen peroxide; In acetic acid; for 75h; Ambient temperature;

Reference yield: 61.0%

: 75745-64-1
5-<(4-nitrophenyl)sulphonyl>-2-furancarbonitrile

: 75745-74-3
5-<(4-nitrophenyl)sulphonyl>-2-furancarboxamide oxime

Guidance literature:: With potassium hydroxide; hydroxylamine hydrochloride; In ethanol; for 3h; Heating;

Reference yield:

: 75745-64-1
5-<(4-nitrophenyl)sulphonyl>-2-furancarbonitrile

: 75745-83-4
2-<(5-(4-nitrophenyl)sulphonyl)-2-furanyl>-imidazoline

Guidance literature:: Multi-step reaction with 2 steps

1: HCl(g) / 48 h / 0 - 5 °C

2: 63 percent / methanol / 8 h / Heating

With hydrogenchloride; In methanol;