Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate

Base Information

Chemical Name:Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate
CAS No.:349552-23-4
Molecular Formula:C₁₃H₁₂N₂O₆S
Molecular Weight:324.314
Hs Code.:
DSSTox Substance ID:DTXSID101207747

Synonyms:Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate;DTXSID101207747;349552-23-4

Suppliers and Price of Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:324.04160728
Heavy Atom Count:22
Complexity:516

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=N)C1=CC=C(O1)S(=O)(=O)C2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate

There total 3 articles about Ethyl 5-[(4-nitrophenyl)sulfonyl]-2-furancarboximidate 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:

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

: 349552-23-4
ethyl 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate

Guidance literature:: Multi-step reaction with 3 steps

1: 54 percent / 46percent H₂O₂ / acetic acid / 75 h / Ambient temperature

2: HCl(g) / 48 h / 0 - 5 °C

3: 3percent aq. NaHCO₃ / 0.5 h / Ambient temperature

With hydrogenchloride; dihydrogen peroxide; sodium hydrogencarbonate; In acetic acid;

Reference yield:

: 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate HCl

: 349552-23-4
ethyl 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate

Guidance literature:: With sodium hydrogencarbonate; for 0.5h; Ambient temperature;

Reference yield:

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

: 349552-23-4
ethyl 5-<(4-nitrophenyl)sulphonyl>-2-furancarboximidate

Guidance literature:: Multi-step reaction with 2 steps

1: HCl(g) / 48 h / 0 - 5 °C

2: 3percent aq. NaHCO₃ / 0.5 h / Ambient temperature

With hydrogenchloride; sodium hydrogencarbonate;