2-(5-Nitrofuran-2-carbonyl)hydrazine-1-carbothioamide

Base Information

• Chemical Name: 2-(5-Nitrofuran-2-carbonyl)hydrazine-1-carbothioamide
• CAS No.: 1673-59-2
• Molecular Formula: C6H6 N4 O4 S
• Molecular Weight: 230.204
• NSC Number: 38625
• DSSTox Substance ID: DTXSID50402333
• Wikidata: Q82205732
• Mol file: 1673-59-2.mol

Synonyms:[(5-nitrofuran-2-carbonyl)amino]thiourea;1673-59-2;2-(5-Nitrofuran-2-carbonyl)hydrazine-1-carbothioamide;NSC38625;DTXSID50402333;CCG-51556;NSC-38625;AKOS014548324;Semicarbazide, 1-(5-nitro-2-furoyl)-3-thio-,;SR-01000640849-1

Chemical Property of 2-(5-Nitrofuran-2-carbonyl)hydrazine-1-carbothioamide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.622g/cm³
• XLogP3: 0.3
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 230.01097586
• Heavy Atom Count: 15
• Complexity: 291

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(OC(=C1)[N+](=O)[O-])C(=O)NNC(=S)N

Technology Process of 2-(5-Nitrofuran-2-carbonyl)hydrazine-1-carbothioamide

There total 1 articles about 2-(5-Nitrofuran-2-carbonyl)hydrazine-1-carbothioamide 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:

→ 1-(5-nitro-furan-2-carbonyl)-thiosemicarbazide (1673-59-2)

Guidance literature:

Thiosemicarbazid, NaHCO3, Dioxan, 5-Nitro-2-furoylchlorid, Raumtemp. (dann Erwaermen );

DOI:10.1021/jo01060a021

Reference yield:

1-(5-nitro-furan-2-carbonyl)-thiosemicarbazide (1673-59-2) → 2-amino-5-(5-nitro-2-furyl)-1,3,4-thiadiazole (712-68-5)

Guidance literature:

With sulfuric acid;

DOI:10.1021/jo01060a021

Reference yield:

1-(5-nitro-furan-2-carbonyl)-thiosemicarbazide (1673-59-2) → 2-Amino-5-(5-nitro-2-furyl)-1,3,4-oxadiazol (3775-55-1)

Guidance literature:

With lead(II,IV) oxide; In ethanol;

DOI:10.1021/jo01060a021

Downstream raw materials:

2-Amino-5-(5-nitro-2-furyl)-1,3,4-oxadiazol

2-amino-5-(5-nitro-2-furyl)-1,3,4-thiadiazole

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