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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-ethyl-2-nitro-

CCNc1ccccc1[N+](=O)[O-] Request for Quotation
Chemical Name: Benzenamine, N-ethyl-2-nitro-
CAS Number: 10112-15-9
Product Number: AG0003SE(AGN-PC-0JLTU7)
Synonyms:
MDL No:
Molecular Formula: C8H10N2O2
Molecular Weight: 166.1772

Identification/Properties

Properties
MP:
92.9°C (estimate)
BP:
168 °C20 mm Hg(lit.)
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.645(lit.)
Computed Properties
Molecular Weight:
166.18g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
166.074g/mol
Monoisotopic Mass:
166.074g/mol
Topological Polar Surface Area:
57.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
156
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#:
N/A
Hazard Statements:
H302-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Ethyl-2-nitroaniline is a versatile compound that finds widespread applications in chemical synthesis. Its unique chemical properties make it a valuable building block in the creation of various organic compounds. In the realm of synthetic chemistry, N-Ethyl-2-nitroaniline serves as a key intermediate in the production of dyes, pharmaceuticals, and agrochemicals. Its ability to undergo various transformations, such as reduction and substitution reactions, makes it a valuable tool for chemists seeking to introduce specific functionalities into their target molecules. Additionally, N-Ethyl-2-nitroaniline can be employed in the preparation of novel materials and as a precursor in the development of catalysts. Its role in chemical synthesis highlights its importance as a versatile and valuable compound in the field of organic chemistry.