(1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine

Base Information

Chemical Name:(1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine
CAS No.:736-53-8
Molecular Formula:C10H6 N4 O6
Molecular Weight:278.181
Hs Code.:
European Community (EC) Number:212-003-6
Mol file:736-53-8.mol

Synonyms:(1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine;736-53-8;F19267

Suppliers and Price of (1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine

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 18 raw suppliers

Chemical Property of (1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine

Chemical Property:

Vapor Pressure:5.69E-07mmHg at 25°C
Melting Point:240-241 °C
Boiling Point:423°C at 760 mmHg
PKA:4.17±0.50(Predicted)
Flash Point:209.6°C
PSA：142.64000
Density:1.63g/cm³
LogP:3.18840
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:3
Exact Mass:278.02873392
Heavy Atom Count:20
Complexity:388

Purity/Quality:: 97% ^*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=NN=CC2=CC=C(O2)[N+](=O)[O-]
Isomeric SMILES:C1=C(OC(=C1)[N+](=O)[O-])/C=N/N=C\C2=CC=C(O2)[N+](=O)[O-]
Uses 5-Nitrofuraldazine Nifuratel(N458250) which is a drug used as an antibacterial, antifungal, antiprotozoal (Trichomonas). Nifuratel appears to have a broad antibacterial spectrum of action and is effective against Chlamydia trachomatis and Mycoplasma spp. as well as fungal infections from Candida spp.

Technology Process of (1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine

There total 5 articles about (1Z)-1,2-Bis((5-nitrofuran-2-yl)methylene)hydrazine 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:

: 13221-86-8
2,4-dihydroxybenzoic acid hydrazide

: 5-nitro-2-furaldehyde diacetate

: 304481-57-0
C₁₂H₉N₃O₆

: 736-53-8
1,2-bis((5-nitrofuran-2-yl)methylene)hydrazine

Guidance literature:: 5-nitro-2-furaldehyde diacetate; With sulfuric acid; In water; at 100 ℃;

2,4-dihydroxybenzoic acid hydrazide; In water; at 100 ℃;
DOI:10.1016/j.molliq.2021.116911

Reference yield:

: 39635-11-5
3,4-dihydroxy-benzoic acid hydrazide

: 5-nitro-2-furaldehyde diacetate

: C₁₂H₉N₃O₆

: 736-53-8
1,2-bis((5-nitrofuran-2-yl)methylene)hydrazine

Guidance literature:: 5-nitro-2-furaldehyde diacetate; With sulfuric acid; In water; at 100 ℃;

3,4-dihydroxy-benzoic acid hydrazide; In water; at 100 ℃;
DOI:10.1016/j.molliq.2021.116911

Reference yield:

: 98-01-1
furfural

: C₁₂H₉N₃O₆

: 736-53-8
1,2-bis((5-nitrofuran-2-yl)methylene)hydrazine

Guidance literature:: Multi-step reaction with 2 steps

1.1: sulfuric acid; nitric acid / 0 - 10 °C

1.2: 0.5 h / 0 - 5 °C

2.1: sulfuric acid / water / 100 °C

2.2: 100 °C

With sulfuric acid; nitric acid; In water;
DOI:10.1016/j.molliq.2021.116911