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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)-

Benzene, 2,4-dibromo-1-iodo-

Brc1ccc(c(c1)Br)I Request for Quotation
Chemical Name: Benzene, 2,4-dibromo-1-iodo-
CAS Number: 19393-94-3
Product Number: AG0037N7(AGN-PC-00MOLO)
Synonyms:
MDL No: MFCD09753709
Molecular Formula: C6H3Br2I
Molecular Weight: 361.8005

Identification/Properties

Properties
MP:
45-46℃
BP:
299.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
361.802g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
0
Exact Mass:
361.763g/mol
Monoisotopic Mass:
359.765g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
97.1
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


2,4-Dibromo-1-iodobenzene is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. As a key building block in organic chemistry, this compound is commonly employed in the preparation of various complex molecules and pharmaceuticals. Its specific application lies in its ability to serve as a valuable intermediate in the synthesis of biologically active compounds through strategic functional group transformations. Furthermore, the presence of both bromine and iodine atoms in its structure provides opportunities for selective reactions and diversification of molecular structures. In organic synthesis, 2,4-Dibromo-1-iodobenzene acts as a crucial reagent facilitating the creation of intricate chemical architectures with precise control over regioselectivity and stereochemistry. Its importance in the advancement of organic chemistry research and drug discovery highlights the significance of this compound as a foundational component in the synthesis of novel molecules with potential therapeutic applications.