2-Furaldehyde, 5-nitro-, 4,4-dimethyl-3-thiosemicarbazone

Base Information

Chemical Name:2-Furaldehyde, 5-nitro-, 4,4-dimethyl-3-thiosemicarbazone
CAS No.:14052-79-0
Molecular Formula:C8H10N4O3S
Molecular Weight:0
Hs Code.:2934999090
DSSTox Substance ID:DTXSID80161426
Mol file:14052-79-0.mol

Synonyms:2-FURALDEHYDE, 5-NITRO-, 4,4-DIMETHYL-3-THIOSEMICARBAZONE;14052-79-0;BRN 1349236;5-Nitro-2-furaldehyde 4,4-dimethyl-3-thiosemicarbazone;1,1-dimethyl-3-[(E)-(5-nitrofuran-2-yl)methylideneamino]thiourea;C8H10N4O3S;C8-H10-N4-O3-S;DTXSID80161426;LS-69928;1,1-dimethyl-3-[(E)-(5-nitro-2-furyl)methyleneamino]thiourea

Suppliers and Price of 2-Furaldehyde, 5-nitro-, 4,4-dimethyl-3-thiosemicarbazone

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

American Custom Chemicals Corporation
5-NITRO-2-FURALDEHYDE 4,4-DIMETHYL-3-THIOSEMICARBAZONE 95.00%
5MG
$ 504.74

Total 2 raw suppliers

Chemical Property of 2-Furaldehyde, 5-nitro-, 4,4-dimethyl-3-thiosemicarbazone

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:350.697°C at 760 mmHg
Flash Point:165.896°C
PSA：125.72000
Density:1.409g/cm³
LogP:1.89230
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:242.04736137
Heavy Atom Count:16
Complexity:302

Purity/Quality:

99% ^*data from raw suppliers

5-NITRO-2-FURALDEHYDE 4,4-DIMETHYL-3-THIOSEMICARBAZONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2-Furaldehyde, 5-nitro-, 4,4-dimethyl-3-thiosemicarbazone

There total 1 articles about 2-Furaldehyde, 5-nitro-, 4,4-dimethyl-3-thiosemicarbazone 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: