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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, N,N-diethyl-3-nitro-

CCN(c1cccc(c1)[N+](=O)[O-])CC Request for Quotation
Chemical Name: Benzenamine, N,N-diethyl-3-nitro-
CAS Number: 2216-16-2
Product Number: AG003SJE(AGN-PC-0JLP6X)
Synonyms:
MDL No:
Molecular Formula: C10H14N2O2
Molecular Weight: 194.2304

Identification/Properties

Properties
BP:
289 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
194.234g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
194.106g/mol
Monoisotopic Mass:
194.106g/mol
Topological Polar Surface Area:
49.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
187
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N-Diethyl-3-nitrobenzenamine is a versatile compound frequently employed in chemical synthesis due to its properties and reactivity. This compound serves as a valuable building block in the development of various organic molecules, particularly in the field of medicinal chemistry. Its nitro group provides a site for further functionalization, enabling the synthesis of a wide range of derivatives with diverse applications. Additionally, the presence of the diethylamine moiety enhances the compound's solubility and compatibility in different reaction conditions, making it an attractive candidate for use in complex synthetic pathways. As a reagent in chemical synthesis, N,N-Diethyl-3-nitrobenzenamine plays a crucial role in creating novel compounds with potential pharmaceutical, agrochemical, and materials science applications.