Nifuraldezone

Base Information

• Chemical Name: Nifuraldezone
• CAS No.: 3270-71-1
• Molecular Formula: C7H6 N4 O5
• Molecular Weight: 226.148
• Hs Code.: 2934999090
• European Community (EC) Number: 221-890-9
• NSC Number: 3184
• NCI Thesaurus Code: C77051
• ChEMBL ID: CHEMBL1358619
• Mol file: 3270-71-1.mol

Synonyms:NIFURALDEZONE;Furamazone;Nifuraldezon;Framazone;N-(5-Nitrofurfurylidenamino)oxamide;NF 84;5-Nitro-2-furaldehyde semioxamazone;component of Aldefur Bolus Veterinary;CBC 503239;5-Nitro-2-furaldehyde semioxazone;NSC-3184;component of Entefur Bolus Veterinary;Nifuraldezone [USAN:INN];Nifuraldezonum [INN-Latin];2-Furaldehyde, 5-nitro-, semioxamazone;Nifuraldezona [INN-Spanish];NSC3184;NSC 3184;EINECS 221-890-9;2-Furaldehyde, 5-nitro-, semioxazone;3270-71-1;BRN 0239535;NCGC00164502-01;NCGC00164502-02;Nifuraldezona;Nifuraldezonum;DTXCID4026399;NF-84;Acetic acid, aminooxo-, [(5-nitro-2-furanyl)methylene]hydrazide;CAS-3270-71-1;UNII-0180PBK4FC;DTXSID6046399;Acetic acid, aminooxo-, ((5-nitro-2-furanyl)methylene)hydrazide;Nifuraldezone (USAN/INN);2-Furaldehyde, semioxamazone;SCHEMBL193102;SCHEMBL193103;CHEMBL1358619;AJSKOLZKIUMPPG-YCRREMRBSA-N;Tox21_112140;CBC503239;AKOS003867361;Tox21_112140_1;LS-69953;D05159;component of Aldefur Bolus Veterinary (Salt/Mix);component of Entefur Bolus Veterinary (Salt/Mix);N'-[(E)-(5-nitro-2-furyl)methyleneamino]oxamide;SR-01000945201;SR-01000945201-1;Z49644633;Aminooxoacetic acid [(5-nitro-2-furanyl)methylene]hydrazide;2-(2-[(5-Nitro-2-furyl)methylene]hydrazino)-2-oxoacetamide #

Chemical Property of Nifuraldezone

Chemical Property:

• Melting Point: 270° (dec)
• PKA: 9.62±0.46(Predicted)
• PSA: 143.51000
• Density: 1.74g/cm³
• LogP: 0.73760
• XLogP3: 0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 226.03381930
• Heavy Atom Count: 16
• Complexity: 336

Purity/Quality:

99% ^*data from raw suppliers

NIFURALDEZONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(OC(=C1)[N+](=O)[O-])C=NNC(=O)C(=O)N
• Isomeric SMILES: C1=C(OC(=C1)[N+](=O)[O-])/C=N/NC(=O)C(=O)N
• Uses: Antibacterial. Nifuraldezone is an antibacterial agent. A topical anti-infective drug.

Technology Process of Nifuraldezone

There total 2 articles about Nifuraldezone 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:

5-nitrofurane-2-carboxaldehyde (698-63-5) + oxalamic acid hydrazide (515-96-8) → 5-nitro-furfural-aminooxalylhydrazone (3270-71-1)

Guidance literature:

With ethanol; water;

Reference yield:

→ 5-nitro-furfural-aminooxalylhydrazone (3270-71-1)

Guidance literature:

upstream raw materials:

5-nitrofurane-2-carboxaldehyde

oxalamic acid hydrazide

Refernces