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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)-

4-Bromo-2-nitro-5-(octyloxy)aniline

[O-][N+](=O)c1cc(Br)c(cc1N)OCCCCCCCC Request for Quotation
Chemical Name: 4-Bromo-2-nitro-5-(octyloxy)aniline
CAS Number: 1255574-47-0
Product Number: AG000NUF(AGN-PC-0WAK9M)
Synonyms:
MDL No:
Molecular Formula: C14H21BrN2O3
Molecular Weight: 345.2321

Identification/Properties

Computed Properties
Molecular Weight:
345.237g/mol
XLogP3:
5.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
344.074g/mol
Monoisotopic Mass:
344.074g/mol
Topological Polar Surface Area:
81.1A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
286
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-2-nitro-5-(octyloxy)aniline is a versatile chemical compound commonly utilized in chemical synthesis processes to introduce specific functional groups into molecules or polymers. This compound serves as an essential building block in the creation of various advanced materials and pharmaceuticals. By incorporating 4-Bromo-2-nitro-5-(octyloxy)aniline into reaction mixtures, chemists can introduce both bromine and nitro groups, along with an octyloxy substituent, at precise locations within a molecule. This allows for the controlled modification of molecular structures, enabling the synthesis of complex organic compounds with tailored properties. Furthermore, the unique reactivity of 4-Bromo-2-nitro-5-(octyloxy)aniline makes it a valuable tool in the development of novel compounds for applications in fields such as organic electronics, materials science, and medicinal chemistry.