2-Nitro-P-phenylenediamine

Base Information

Chemical Name:2-Nitro-P-phenylenediamine
CAS No.:183870-67-9
Deprecated CAS:29467-01-4
Molecular Formula:C₆H₇N₃O₂
Molecular Weight:153.14
Hs Code.:
European Community (EC) Number:226-164-5
ICSC Number:1542
NSC Number:5377
UN Number:1673
UNII:PV83F3C01Q
DSSTox Substance ID:DTXSID4020957
Nikkaji Number:J3.720F
Wikidata:Q26840737
ChEMBL ID:CHEMBL353971
Mol file:183870-67-9.mol

Synonyms:1,4-diamino-2-nitrobenzene;2-nitro-1,4-phenylenediamine;2-nitro-4-phenylenediamine;2-nitro-4-phenylenediamine dihydrochloride;2-nitro-4-phenylenediamine sulfate (1:1);2-nitro-p-phenylenediamine;o-nitro-p-phenylenediamine

Suppliers and Price of 2-Nitro-P-phenylenediamine

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 1 raw suppliers

Chemical Property of 2-Nitro-P-phenylenediamine

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:153.053826475
Heavy Atom Count:11
Complexity:156
Transport DOT Label:Poison

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Chemical Classes:Nitrogen Compounds -> Nitroanilines
Canonical SMILES:C1=CC(=C(C=C1N)[N+](=O)[O-])N
Inhalation Risk:No indication can be given about the rate at which a harmful concentration of this substance in the air is reached on evaporation at 20 °C.
Effects of Long Term Exposure:Repeated or prolonged contact may cause skin sensitization.

Technology Process of 2-Nitro-P-phenylenediamine

There total 3 articles about 2-Nitro-P-phenylenediamine 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: 80.0%

: 2871-01-4
1-[(2-hydroxyethyl)amino]-2-nitro-4-aminobenzene

: 119-34-6
4-amino-2-nitrophenol

: 5307-14-2,183870-67-9
2-nitro-1,4-phenylenediamine

Guidance literature:: With ammonium hydroxide; sodium sulfite; for 72h; Product distribution; Na₂SO₃ catalysis, influence of time, solvent;
DOI:10.1016/S0040-4020(98)00181-1