1,3-Benzenedicarboxaldehyde, 4,6-dinitro-

Base Information

Chemical Name:1,3-Benzenedicarboxaldehyde, 4,6-dinitro-
CAS No.:65924-59-6
Molecular Formula:C8H4N2O6
Molecular Weight:224.13
Hs Code.:
DSSTox Substance ID:DTXSID10372780
Nikkaji Number:J2.429.681D
Wikidata:Q82160654

Synonyms:1,3-Benzenedicarboxaldehyde, 4,6-dinitro-;65924-59-6;4,6-Dinitroisophthalaldehyde;SCHEMBL9215364;DTXSID10372780;AKOS004905032

Suppliers and Price of 1,3-Benzenedicarboxaldehyde, 4,6-dinitro-

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 9 raw suppliers

Chemical Property of 1,3-Benzenedicarboxaldehyde, 4,6-dinitro-

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:2
Exact Mass:224.00693585
Heavy Atom Count:16
Complexity:290

Purity/Quality:: 99% ,98%,Electron Grade , ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C(=CC(=C1C=O)[N+](=O)[O-])[N+](=O)[O-])C=O

Technology Process of 1,3-Benzenedicarboxaldehyde, 4,6-dinitro-

There total 7 articles about 1,3-Benzenedicarboxaldehyde, 4,6-dinitro- 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: 54.0%

: 67640-41-9
C₂₄H₂₄N₆O₆

: 65924-59-6
4,6-dinitro-1,3-benzenedicarboxaldehyde

Guidance literature:: With sulfuric acid; In toluene; at 65 ℃;
DOI:10.1139/V06-094

Reference yield:

: 616-72-8
4,6-dinitro-m-xylene

: 65924-59-6
4,6-dinitro-1,3-benzenedicarboxaldehyde

Guidance literature:: Yield given. Multistep reaction;

Reference yield:

: 4,6-Dinitro-1,3-bis--benzol

: 65924-59-6
4,6-dinitro-1,3-benzenedicarboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / aq. NaOH / ethanol / -5 - 5 °C

2: 54 percent / aq. H₂SO₄ / toluene / 65 °C

With sodium hydroxide; sulfuric acid; In ethanol; toluene;
DOI:10.1139/V06-094