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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, 3,5-dibromo-4-methyl-

Nc1cc(Br)c(c(c1)Br)C Request for Quotation
Chemical Name: Benzenamine, 3,5-dibromo-4-methyl-
CAS Number: 13194-73-5
Product Number: AG000ZYC(AGN-PC-0LW6SJ)
Synonyms:
MDL No:
Molecular Formula: C7H7Br2N
Molecular Weight: 264.9452

Identification/Properties

Computed Properties
Molecular Weight:
264.948g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
264.892g/mol
Monoisotopic Mass:
262.895g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
106
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 3,5-Dibromo-4-methylaniline in chemical synthesis lies in its role as a versatile building block for the creation of various organic compounds. This compound is commonly used as a precursor in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its unique chemical structure allows for selective functionalization at specific positions, making it valuable in the creation of complex molecules. Additionally, 3,5-Dibromo-4-methylaniline can participate in cross-coupling reactions, substitution reactions, and other transformations to introduce new functional groups into molecules, expanding the scope of synthetic possibilities in organic chemistry.