1. Home
  2. Benzenamine, 4-nitro-N-(4-nitrophenyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Benzenamine, 4-nitro-N-(4-nitrophenyl)-

[O-][N+](=O)c1ccc(cc1)Nc1ccc(cc1)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzenamine, 4-nitro-N-(4-nitrophenyl)-
CAS Number: 1821-27-8
Product Number: AG0023D3(AGN-PC-0JOC1S)
Synonyms:
MDL No:
Molecular Formula: C12H9N3O4
Molecular Weight: 259.2176

Identification/Properties

Properties
MP:
216 °C
BP:
402.47°C (rough estimate)
Storage:
Room Temperature;
Form:
Solid
Refractive Index:
1.5700 (estimate)
Computed Properties
Molecular Weight:
259.221g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
259.059g/mol
Monoisotopic Mass:
259.059g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
291
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Bis(4-nitrophenyl)amine is a versatile compound widely used in chemical synthesis. Its unique chemical properties make it a valuable reagent in various reactions, including organic synthesis, pharmaceutical development, and material science. When employed in chemical reactions, Bis(4-nitrophenyl)amine serves as a key building block for creating complex molecules and functional materials. Its ability to undergo selective transformations and form stable intermediates makes it an essential tool for synthesizing diverse compounds with precise structural control. By facilitating the formation of specific chemical bonds and enabling the modification of molecular properties, Bis(4-nitrophenyl)amine plays a crucial role in advancing research and development across different scientific disciplines.