Oxalimidohydrazide

Base Information

Chemical Name:Oxalimidohydrazide
CAS No.:3457-37-2
Molecular Formula:C2H8 N6
Molecular Weight:116.126
Hs Code.:
European Community (EC) Number:222-386-1
NSC Number:48226
Mol file:3457-37-2.mol

Synonyms:Oxalimidohydrazide;Diimidooxalic acid dihydrazide;Oxalamidrazone;3457-37-2;Oxalic acid bisamidrazone;Diimidooxalic acid hydrazide;Oxalimidic acid, dihydrazide;Diimidoxalic acid dihydrazide;Ethanediimidic acid, dihydrazide;NSC48226;oxalohydrazide diimide;(1Z,2Z)-ethanedihydrazonamide;EINECS 222-386-1;NSC 48226;NSC-48226;STK260071;AKOS004118342;AKOS024364105

Suppliers and Price of Oxalimidohydrazide

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

TRC
EthanediimidicAcid1,2-Dihydrazide
1g
$ 1260.00

Total 7 raw suppliers

Chemical Property of Oxalimidohydrazide

Chemical Property:

Vapor Pressure:1.03E-05mmHg at 25°C
Boiling Point:371.5°Cat760mmHg
Flash Point:178.5°C
PSA：128.80000
Density:1.9g/cm³
LogP:0.24940
XLogP3:-0.6
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:116.08104428
Heavy Atom Count:8
Complexity:107

Purity/Quality:

99% ^*data from raw suppliers

EthanediimidicAcid1,2-Dihydrazide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(=NN)(C(=NN)N)N
Isomeric SMILES:C(=N\N)(\N)/C(=N/N)/N
Uses Ethanediimidic Acid 1,2-Dihydrazide is used as a reagent in the synthesis of aryl(pyridyl)triazines as extractants for partitioning actinium and europium.

Technology Process of Oxalimidohydrazide

There total 9 articles about Oxalimidohydrazide 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: 96.0%