2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)sulfonyl)-

Base Information

Chemical Name:2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)sulfonyl)-
CAS No.:75745-73-2
Molecular Formula:C₁₂H₁₂N₂O₅S
Molecular Weight:296.304
Hs Code.:
DSSTox Substance ID:DTXSID30226635
Mol file:75745-73-2.mol

Synonyms:BRN 4502714;2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)sulfonyl)-;75745-73-2;N-Hydroxy-5-((4-methoxyphenyl)sulfonyl)-2-furancarboximidamide;C12-H12-N2-O5-S;DTXSID30226635;LS-70149

Suppliers and Price of 2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)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

Total 1 raw suppliers

Chemical Property of 2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)sulfonyl)-

Chemical Property:

Boiling Point:568.48oC at 760 mmHg
Flash Point:297.606oC
PSA：123.50000
Density:1.481g/cm3
LogP:2.99660
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:296.04669266
Heavy Atom Count:20
Complexity:451

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(O2)C(=NO)N
Isomeric SMILES:COC1=CC=C(C=C1)S(=O)(=O)C2=CC=C(O2)/C(=N\O)/N

Technology Process of 2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)sulfonyl)-

There total 2 articles about 2-Furancarboximidamide, N-hydroxy-5-((4-methoxyphenyl)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: 55.0%

: 75745-63-0
5-<(4-methoxyphenyl)sulphonyl>-2-furancarbonitrile

: 75745-73-2
5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxamide oxime

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

Reference yield:

: 61942-33-4
5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxaldehyde

: 75745-73-2
5-<(4-methoxyphenyl)sulphonyl>-2-furancarboxamide oxime

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / NH₂OH*HCl, Ac₂O / methanol / 1 h / Heating

2: 55 percent / NH₂OH*HCl, KOH / ethanol / 3 h / Heating

With potassium hydroxide; hydroxylamine hydrochloride; acetic anhydride; In methanol; ethanol;