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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, 2,6-dibromo-4-chloro-

Clc1cc(Br)c(c(c1)Br)N Request for Quotation
Chemical Name: Benzenamine, 2,6-dibromo-4-chloro-
CAS Number: 874-17-9
Product Number: AG004JA3(AGN-PC-0JTZYW)
Synonyms:
MDL No:
Molecular Formula: C6H4Br2ClN
Molecular Weight: 285.3637

Identification/Properties

Properties
MP:
94-96 °C(lit.);
BP:
297.4 °C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
285.363g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
284.838g/mol
Monoisotopic Mass:
282.84g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


Benzenamine, 2,​6-​dibromo-​4-​chloro- is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in various reactions due to its unique structure and properties. In organic synthesis, Benzenamine, 2,​6-​dibromo-​4-​chloro- can act as a key building block for the construction of complex molecules. Its bromine and chlorine substituents enable selective functionalization at specific positions within an aromatic ring, making it valuable for designing and modifying organic compounds. Additionally, this compound is frequently employed in the development of pharmaceuticals, agrochemicals, and materials with tailored properties. Its ability to undergo diverse chemical transformations makes Benzenamine, 2,​6-​dibromo-​4-​chloro- a valuable tool for synthetic chemists seeking to create novel molecules with desired functions.