Hydrazinecarboxamide, 1-[2-(dimethylamino)ethyl]-2-[(5-nitro-2-furanyl)methylene]-

Base Information

• Chemical Name: Hydrazinecarboxamide, 1-[2-(dimethylamino)ethyl]-2-[(5-nitro-2-furanyl)methylene]-
• CAS No.: 5580-25-6
• Molecular Formula: C₁₀H₁₅N₅O₄
• Molecular Weight: 269.26
• NSC Number: 6487
• Wikidata: Q27264334
• Mol file: 5580-25-6.mol

Synonyms:Hydrazinecarboxamide, 1-[2-(dimethylamino)ethyl]-2-[(5-nitro-2-furanyl)methylene]-;5580-25-6;1-[2-(dimethylamino)ethyl]-1-[(Z)-(5-nitrofuran-2-yl)methylideneamino]urea;Nifuramizonum;Nifurethazon;NSC6487;NF 189;Q27264334;2-Furaldehyde, 2-[2-(dimethylamino)ethyl]semicarbazone

Chemical Property of Hydrazinecarboxamide, 1-[2-(dimethylamino)ethyl]-2-[(5-nitro-2-furanyl)methylene]-

Chemical Property:

• Vapor Pressure: 5.21E-07mmHg at 25°C
• Boiling Point: 412.4°Cat760mmHg
• Flash Point: 203.2°C
• PSA: 120.89000
• Density: 1.37g/cm³
• LogP: 1.68750
• XLogP3: 0.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 269.11240398
• Heavy Atom Count: 19
• Complexity: 354

Purity/Quality:

99% ^*data from raw suppliers

NIFURETHAZONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)CCN(C(=O)N)N=CC1=CC=C(O1)[N+](=O)[O-]
• Isomeric SMILES: CN(C)CCN(C(=O)N)/N=C\C1=CC=C(O1)[N+](=O)[O-]

Technology Process of Hydrazinecarboxamide, 1-[2-(dimethylamino)ethyl]-2-[(5-nitro-2-furanyl)methylene]-

There total 2 articles about Hydrazinecarboxamide, 1-[2-(dimethylamino)ethyl]-2-[(5-nitro-2-furanyl)methylene]- 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) → 5-Nitrofurfural-(2)-2-(2-dimethylaminoethyl)-semicarbazon (5580-25-6)

Guidance literature:

With hydrogenchloride; potassium cyanate; potassium hydroxide; Reagens 4: Aethanol;

Reference yield:

→ 5-Nitrofurfural-(2)-2-(2-dimethylaminoethyl)-semicarbazon (5580-25-6)

Guidance literature:

2-(2-Dimethylaminoethyl)-semicarbazid, 5-Nitro-furfural-(2), wss. A.;

DOI:10.1021/jo01032a022

upstream raw materials:

5-nitrofurane-2-carboxaldehyde

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