5-(5-Nitro-2-furyl)-1,3,4-oxadiazole-2-thiol

Base Information

Chemical Name:5-(5-Nitro-2-furyl)-1,3,4-oxadiazole-2-thiol
CAS No.:94646-96-5
Molecular Formula:C₆H₃N₃O₄S
Molecular Weight:213.174
Hs Code.:2934999090
DSSTox Substance ID:DTXSID90369517
Mol file:94646-96-5.mol

Synonyms:5-(5-nitro-2-furyl)-1,3,4-oxadiazole-2-thiol;94646-96-5;5-(5-nitrofuran-2-yl)-3H-1,3,4-oxadiazole-2-thione;5-(5-Nitrofuran-2-yl)-1,3,4-oxadiazole-2-thiol;Maybridge1_006718;HMS560J08;DTXSID90369517;CCG-51793;SR-01000641072-1

Suppliers and Price of 5-(5-Nitro-2-furyl)-1,3,4-oxadiazole-2-thiol

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

CHESS?
MC002875:5-(5-Nitro-furan-2-yl)-[1,3,4]oxadiazole-2-thiol 95
1 g
$ 336.00

American Custom Chemicals Corporation
5-(5-NITRO-2-FURYL)-1,3,4-OXADIAZOLE-2-THIOL 95.00%
10G
$ 1365.68

American Custom Chemicals Corporation
5-(5-NITRO-2-FURYL)-1,3,4-OXADIAZOLE-2-THIOL 95.00%
1G
$ 652.22

Total 5 raw suppliers

Chemical Property of 5-(5-Nitro-2-furyl)-1,3,4-oxadiazole-2-thiol

Chemical Property:

Vapor Pressure:0.000592mmHg at 25°C
Refractive Index:1.812
Boiling Point:310.7°Cat760mmHg
Flash Point:141.7°C
PSA：136.68000
Density:1.96g/cm³
LogP:2.04970
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:212.98442676
Heavy Atom Count:14
Complexity:313

Purity/Quality:

99% ^*data from raw suppliers

MC002875:5-(5-Nitro-furan-2-yl)-[1,3,4]oxadiazole-2-thiol 95 ^*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-])C2=NNC(=S)O2

Technology Process of 5-(5-Nitro-2-furyl)-1,3,4-oxadiazole-2-thiol

There total 1 articles about 5-(5-Nitro-2-furyl)-1,3,4-oxadiazole-2-thiol 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:

: 94646-96-5
5-(5-Nitro-2-furyl)-1,3,4-oxadiazol-2-thion

Guidance literature:: 5-Nitro-2-furoyl-hydrazin/Dioxan, Thiophosgen , Ausb. 64percent;
DOI:10.1021/jo01060a021

Reference yield:

: 94646-96-5
5-(5-nitro-2-furyl)-1,3,4-oxadiazol-2-thiol

: 135264-42-5
[5-(5-Nitro-furan-2-yl)-[1,3,4]oxadiazol-2-ylsulfanyl]-acetic acid [1-phenyl-meth-(E)-ylidene]-hydrazide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaHCO₃ / 1.) H₂O, 2.) MeOH, 1 h

2: 6.22 g / hydrazine / benzene; methanol / 0.5 h / 0 °C

3: 83 percent / ethanol / 0.5 h / Heating

With sodium hydrogencarbonate; hydrazine; In methanol; ethanol; benzene;
DOI:10.1002/jps.2600800610

Reference yield:

: 94646-96-5
5-(5-nitro-2-furyl)-1,3,4-oxadiazol-2-thiol

: 135264-40-3
N-salicylidene-α-<5-(5-nitro-2-furyl)-1,3,4-oxadiazol-2-ylthio>acethydrazide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaHCO₃ / 1.) H₂O, 2.) MeOH, 1 h

2: 6.22 g / hydrazine / benzene; methanol / 0.5 h / 0 °C

3: 83 percent / ethanol / 0.5 h / Heating

With sodium hydrogencarbonate; hydrazine; In methanol; ethanol; benzene;
DOI:10.1002/jps.2600800610