4-Nitrobenzene-1,2-diamine dihydrochloride

Base Information

• Chemical Name: 4-Nitrobenzene-1,2-diamine dihydrochloride
• CAS No.: 6219-77-8
• Molecular Formula: C₆H₇N₃O₂*ClH
• Molecular Weight: 189.601
• European Community (EC) Number: 228-293-2
• UNII: 10T46XHE84
• DSSTox Substance ID: DTXSID8064141
• Wikidata: Q27251158
• Mol file: 6219-77-8.mol

Synonyms:4-Nitrobenzene-1,2-diamine dihydrochloride;6219-77-8;Fourrine 4G;HSDB 6234;1,2-Benzenediamine, 4-nitro-, dihydrochloride;1,2-Benzenediamine, 4-nitro-, hydrochloride (1:2);UNII-10T46XHE84;4-nitrobenzene-1,2-diamine;dihydrochloride;4-Nitro-o-phenylenediamine HCl;o-Phenylenediamine, 4-nitro-, dihydrochloride;10T46XHE84;EINECS 228-293-2;4-nitro-o-phenylenediamine dihydrochloride;4-NITRO-1,2-BENZENEDIAMINE DIHYDROCHLORIDE;SCHEMBL970605;DTXSID8064141;C.I. 76021;Q27251158;4-NITRO-O-PHENYLENEDIAMINE DIHYDROCHLORIDE [INCI];4-NITRO-1,2-BENZENEDIAMINE DIHYDROCHLORIDE [HSDB];4- nitrobenzene- 1, 2- diamine dihydrochloride (CI 76020)

Chemical Property of 4-Nitrobenzene-1,2-diamine dihydrochloride

Chemical Property:

• Vapor Pressure: 2.68E-07mmHg at 25°C
• Boiling Point: 421.1°C at 760 mmHg
• Flash Point: 208.5°C
• PSA: 97.86000
• LogP: 4.04880
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 225.0071819
• Heavy Atom Count: 13
• Complexity: 156

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Nitrogen Compounds -> Other Aromatics (Nitrogen)
• Canonical SMILES: C1=CC(=C(C=C1[N+](=O)[O-])N)N.Cl.Cl

Technology Process of 4-Nitrobenzene-1,2-diamine dihydrochloride

There total 1 articles about 4-Nitrobenzene-1,2-diamine dihydrochloride 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:

4-Nitrophenylene-1,2-diamine (99-56-9) → 2-amino-5-nitroanilinium chloride (6219-77-8,53209-19-1)

Guidance literature:

With hydrogenchloride; In ethanol;

DOI:10.1107/S2053229614013485

Reference yield:

acetone (67-64-1) + 4-nitro-o-phenylenediamine dihydrochloride (6219-77-8,53209-19-1) → N1,N2-Diisopropylidene-4-nitro-benzene-1,2-diamine

Guidance literature:

With sodium hydroxide; Heating;

upstream raw materials:

4-Nitrophenylene-1,2-diamine

Refernces